Entry - #262890 - SCOTT SYNDROME; SCTS - OMIM - (OMIM.ORG)

# 262890

SCOTT SYNDROME; SCTS


Alternative titles; symbols

BLEEDING DISORDER, PLATELET-TYPE, 7; BDPLT7
BLEEDING ABNORMALITY DUE TO DEFICIENCY OF PLATELET BINDING OF FACTOR X
PROTHROMBIN CONVERSION DEFECT, FAMILIAL
PROTHROMBIN CONSUMPTION DEFICIENCY
PROTHROMBIN CONSUMPTION INHIBITOR, FAMILIAL


Phenotype-Gene Relationships

Location Phenotype Phenotype
MIM number
Inheritance Phenotype
mapping key
Gene/Locus Gene/Locus
MIM number
12q12 Scott syndrome 262890 AR 3 ANO6 608663
Clinical Synopsis
 
Phenotypic Series
 

INHERITANCE
- Autosomal recessive
HEMATOLOGY
- Hemorrhagic diathesis (bleeding tendency)
- Platelet receptor deficiency
- Defect in stimulated platelet capacity to expose surface phosphatidylserine
- Impaired factor Va binding
- Impaired factor VIIIa binding
- Prothrombin activation deficiency
- Factor X activation deficiency
PRENATAL MANIFESTATIONS
Delivery
- Risk of life-threatening postpartum hemorrhage
MISCELLANEOUS
- Patients rarely experience spontaneous bleeding
MOLECULAR BASIS
- Caused by mutation in the anoctamin-6 gene (ANO6, 608663.0001)
Bleeding disorder, platelet-type - PS231200 - 28 Entries
Location Phenotype Inheritance Phenotype
mapping key
Phenotype
MIM number
Gene/Locus Gene/Locus
MIM number
1p36.12 ?Bleeding disorder, platelet-type, 22 AR 3 618462 EPHB2 600997
3p21.31 Gray platelet syndrome AR 3 139090 NBEAL2 614169
3q21.3 Bernard-Soulier syndrome, type C AR 3 231200 GP9 173515
3q25.1 Bleeding disorder, platelet-type, 8 AR 3 609821 P2RY12 600515
5q11.2 Bleeding disorder, platelet-type, 9 AD 2 614200 BDPLT9 614200
7q21.11 Platelet glycoprotein IV deficiency AR 3 608404 CD36 173510
7q34 Bleeding disorder, platelet-type, 14 AD 2 614158 BDPLT14 614158
9q21.11 ?Bleeding disorder, platelet-type, 19 AR 3 616176 PRKACG 176893
9q34.13 Bleeding disorder, platelet-type, 17 AD, AR 3 187900 GFI1B 604383
10q22.2 Quebec platelet disorder AD 3 601709 PLAU 191840
11q13.1 Bleeding disorder, platelet-type, 18 AR 3 615888 RASGRP2 605577
11q24.3 Bleeding disorder, platelet-type, 21 AD, AR 3 617443 FLI1 193067
12q12 Scott syndrome AR 3 262890 ANO6 608663
14q24.1 Bleeding disorder, platelet-type, 15 AD 3 615193 ACTN1 102575
17p13.2 Bernard-Soulier syndrome, type A1 (recessive) AR 3 231200 GP1BA 606672
17p13.2 von Willebrand disease, platelet-type AD 3 177820 GP1BA 606672
17q12 Bleeding disorder, platelet-type, 20 AD 3 616913 SLFN14 614958
17q21.31 Bleeding disorder, platelet-type, 16, autosomal dominant AD 3 187800 ITGA2B 607759
17q21.31 Glanzmann thrombasthenia 1 AR 3 273800 ITGA2B 607759
17q21.32 Bleeding disorder, platelet-type, 24, autosomal dominant AD 3 619271 ITGB3 173470
17q21.32 Glanzmann thrombasthenia 2 AR 3 619267 ITGB3 173470
19p13.3 {Bleeding disorder, platelet-type, 13, susceptibility to} AD 3 614009 TBXA2R 188070
19p13.12-p13.11 Bleeding disorder, platelet-type, 25 AD 3 620486 TPM4 600317
19q13.42 Bleeding disorder, platelet-type, 11 AR 3 614201 GP6 605546
22q11.21 Bernard-Soulier syndrome, type B AR 3 231200 GP1BB 138720
22q11.21 Giant platelet disorder, isolated AR 3 231200 GP1BB 138720
22q12.3 Macrothrombocytopenia and granulocyte inclusions with or without nephritis or sensorineural hearing loss AD 3 155100 MYH9 160775
Not Mapped Bleeding disorder, platelet-type, 12 AD 605735 BDPLT12 605735

TEXT

A number sign (#) is used with this entry because of evidence that Scott syndrome (SCTS) is caused by homozygous or compound heterozygous mutation in the TMEM16F gene (ANO6; 608663) on chromosome 12q12.


Description

Scott syndrome (SCTS) is a mild platelet-type bleeding disorder characterized by impaired surface exposure of procoagulant phosphatidylserine (PS) on platelets and other blood cells, following activation with Ca(2+)-elevating agents (Munnix et al., 2003).

For a discussion of genetic heterogeneity of platelet-type bleeding disorder (BDPLT), see 231200.


Clinical Features

In 4 generations of a family (with 1 instance of male-to-male transmission), Robinson et al. (1967) described a mild bleeding disorder with no spontaneous hemorrhage. Analysis of blood coagulation in 2 generations revealed normal values for all clotting factors and other hemostatic systems except prothrombin consumption and thromboplastin inactivation. Robinson et al. (1967) demonstrated the presence of what they termed an 'inactivator' of active factor X (F10; 613872) in the plasma of these patients which accelerated the decay of blood thromboplastin. The inhibitor resembled that commonly observed in systemic lupus erythematosus; a similar agent was found in normal plasma but in much smaller amounts.

Parry et al. (1980) studied 10 individuals from 3 unrelated Welsh families who had reduced prothrombin conversion as shown by a grossly abnormal prothrombin consumption index (PCI). Male-to-male transmission was reported. All known plasma coagulation factors were present in adequate concentrations; some affected persons had mild postoperative or postpartum bleeding but none suffered spontaneous bleeding. In therapeutic trials both plasma and platelet transfusions were needed to correct the abnormality. This finding, together with in vitro and other in vivo studies, suggested to Parry et al. (1980) that the abnormality was associated with an inhibitor of the interaction between plasma and phospholipid during blood coagulation. Parry et al. (1980) considered the abnormality similar but not identical to that in several members of the family reported by Robinson et al. (1967).

Kojima et al. (1994) demonstrated that the coagulant nonresponder phenotype observed in platelets and erythrocytes in Scott syndrome is expressed by all of the EBV-transformed lymphoblasts derived from the B cells of the patient, and that the unique phenotype of the defective cells can be isolated by single cell cloning and propagated in culture through many generations. The continuous expression of the aberrant phenotype through in vitro culture confirmed that the Scott syndrome defect represents a gene deletion or mutation that is passed to daughter cells through mitosis. Furthermore, they demonstrated by heterokaryon hybridoma fusion that the abnormal Scott phenotype can be corrected by fusion with a cell exhibiting the normal coagulant-responder phenotype, and that the normal phenotype is sustained when these hybridomas are subsequently propagated through many generations. Taken together with the results of previous studies, these data suggested that the cellular defect in Scott syndrome reflects a mutation or deletion of a gene required for normal Ca(2+)-dependent transbilayer migration of phosphatidylserine to the plasma membrane surface and that this defect is shared among the blood cells of lymphoid, megakaryocytic, and erythroid lineages.

Toti et al. (1996) characterized a familial instance of Scott syndrome and confirmed that it is a genetic disorder affecting the outward transmembrane migration of phosphatidylserine. Low prothrombin consumption in the serum of the proposita, a 71-year-old woman, and 2 of her children was the sole abnormal hemostasis parameter. The degree of exposure of procoagulant phospholipids, chiefly phosphatidylserine, was reduced in stimulated platelets, erythrocytes, and EBV-infected B lymphocytes, indicating that multiple hematologic lineages are affected in this disorder. The data were considered compatible with homozygous status of the proposita and heterozygous status of her children. Toti et al. (1996) concluded that Scott syndrome is transmitted as an autosomal recessive trait, reflecting the deletion or mutation of a putative outward phosphatidylserine translocase.

Boisseau et al. (2018) reported 2 sibs with Scott syndrome who were identified due to bleeding during surgery. Ionophore activation of platelets from the patients demonstrated low phosphatidylserine expression.

Bouchaib et al. (2023) reported a 36-year-old Moroccan woman, born of consanguineous parents, who developed a palatal hematoma after dental extraction, had an episode of uterine bleeding, and experienced a miscarriage at 2 months in a pregnancy that was complicated by prolonged uterine bleeding. Laboratory evaluation after the miscarriage revealed a defect in phospholipid scramblase, and the diagnosis of Scott syndrome was confirmed by flow cytometry showing absent or reduced phosphatidylserine on the platelet surface. A second pregnancy 5 years later was uneventful; with the support of preventive measures during delivery, including intravenous antifibrinolytic agents as well as transfusions of platelets and red blood cells, she gave birth to a healthy boy. The authors stated that in published reports of 5 patients with Scott syndrome who had given birth, all experienced postpartum hemorrhage requiring hysterectomy for hemostasis, and there were 2 maternal deaths. The authors recommended that, given the high risk for postpartum hemorrhage, a multidisciplinary team and preventive measures should be available for pregnancy and delivery in women with Scott syndrome.

Reviews

See review of Scott syndrome by Weiss (1994).


Biochemical Features

Miletich et al. (1977, 1978) demonstrated that each platelet has about 200 binding sites with high affinity specifically for activated factor X (factor Xa). Bound factor Xa is 300,000 times more active than free factor Xa in generating thrombin from prothrombin and is protected from inactivation by antithrombin III. Factor V (612309) is also essential for the binding process. The important physiologic role of the platelet receptor for factor X was indicated by the studies (Miletich et al., 1979) of a woman with a hemorrhagic diathesis due to deficiency of the platelet receptor who was first reported by Weiss et al. (1979). Receptors in the parents were normal; however, Miletich et al. (1979) did not exclude autosomal recessive inheritance. Since the patient's value for factor X binding was 25% of normal, the heterozygous state might be characterized by values 75% of normal, which would be indistinguishable from the normal range. Rosing et al. (1985) confirmed the deficiency in capacity to promote prothrombin activation in this patient and demonstrated a deficiency in the ability to promote factor X activation as well. Rosing et al. (1985) also showed that the platelets were defective in the capacity to expose phosphatidylserine at the outer surface of stimulated platelets. In further studies of the same patient, Ahmad et al. (1989) described findings suggesting impairment of factor VIIIa binding.

Phospholipid scramblase (see 604170) is a plasma membrane protein purified by Basse et al. (1996) that mediates accelerated transbilayer migration of phospholipids upon binding calcium ions, facilitating rapid mobilization of phosphatidylserine to the cell surface upon elevation of internal Ca(2+). In patients with Scott syndrome, circulating blood cells show decreased cell surface exposure of phosphatidylserine at elevated cytosolic levels of calcium ion, implying an underlying defect or deficiency of phospholipid scramblase. To gain insight into the molecular basis of Scott syndrome, Stout et al. (1997) compared PL scramblase in Scott erythrocyte membranes to those of normal controls. Whereas membranes of Scott cells were unresponsive to Ca(2+)-induced activation of PL scramblase at neutral pH, apparently normal PL scramblase activity was induced at pH less than 6.0. After extraction with octylglucoside, a membrane protein was isolated from the Scott cells that exhibited normal PL scramblase activity when reconstituted in vesicles with exogenous PLs. Like PL scramblase from normal red cells, PL scramblase from Scott red cells was maximally activated by addition of calcium ion (at pH 7.4) or by acidification to pH less than 6.0, and similar apparent affinities for calcium ion and rates of transbilayer transfer of PLs were observed. Stout et al. (1997) suggested that the defect in Scott syndrome is related to an altered interaction of calcium ion with PL scramblase on the endofacial surface of the cell membrane, due either to an intrinsic constraint upon the protein preventing interaction with calcium ion in situ, or to an unidentified inhibitor or cofactor in the Scott cell that is dissociated by detergent.

Munnix et al. (2003) analyzed the relationship between Ca(2+) flux and phosphatidylserine exposure in platelets and B lymphocytes derived from the original Scott syndrome patient (Weiss et al., 1979), a patient from one of the Welsh families reported by Parry et al. (1980), and 2 controls. The 34-year-old Welsh woman, who had a history of excessive bleeding after dental extractions since childhood, suffered life-threatening postpartum hemorrhage after an uncomplicated forceps delivery. Munnix et al. (2003) found that although she had normal levels of coagulation factors and normal platelet aggregation, her collagen-activated platelets showed only 52% of the prothrombinase activity of a control and had markedly reduced phosphatidylserine exposure, confirming the phenotype of Scott syndrome. Ca(2+) entry into platelets and lymphoblasts from both patients was normal, and elevated intracellular free Ca(2+) concentrations resulting from store-mediated Ca(2+) entry was not sufficient to trigger phosphatidylserine exposure.


Inheritance

The transmission pattern of SCTS in the family reported by Suzuki et al. (2010) was consistent with autosomal recessive inheritance.


Molecular Genetics

Suzuki et al. (2010) identified homozygosity for a splice site mutation in the TMEM16F gene (608663.0001) in the patient with Scott syndrome reported by Weiss et al. (1979) and Kojima et al. (1994).

In 2 sibs with Scott syndrome, Boisseau et al. (2018) identified compound heterozygous mutations in the ANO6 gene (608663.0002-608663.0003). The mutations were identified by Sanger sequencing of the ANO6 gene and copy number analysis from next-generation sequencing data.

By sequencing of the ANO6 gene in a Welsh woman with Scott syndrome, Castoldi et al. (2011) identified compound heterozygous mutations (608663.0004-608773.0005).

By high-throughput sequencing in a 36-year-old Moroccan woman with Scott syndrome, born of consanguineous parents, Bouchaib et al. (2023) identified homozygosity for a nonsense mutation in the ANO6 gene (R440X; 608663.0006). The authors noted that Scott syndrome is likely underdiagnosed, given the relatively benign clinical presentation of most patients.


Nomenclature

The bleeding disorder in the patient studied by Weiss et al. (1979) was referred to as Scott syndrome, presumably on the basis of the patient's surname (Ahmad et al., 1989).


Animal Model

Brooks et al. (2002) discovered a novel canine hereditary bleeding disorder with the characteristic features of Scott syndrome. Affected dogs were from a single, inbred colony and experienced clinical signs of epistaxis, hyphema (hemorrhage into the anterior chamber of the eye), intramuscular hematoma, and prolonged bleeding with cutaneous bruising after surgery. The hemostatic abnormalities were restricted to tests of platelet procoagulant activity, whereas platelet count, platelet morphology under light microscopy, bleeding time, clot retraction, and platelet aggregation and secretion in response to thrombin, collagen, and adenosine diphosphate stimulation were all within normal limits. Washed platelets from the affected dogs demonstrated approximately twice normal clotting times in a platelet factor-3 availability assay and, in a prothrombinase assay, generated only background levels of thrombin in response to calcium ionophore, thrombin, or combined thrombin plus collagen stimulation. These studies indicated recessive inheritance.


History

In a patient with Scott syndrome, Albrecht et al. (2005) identified a heterozygous missense mutation (arg1925 to gln) in the ABCA1 gene (600046), which was not found in unaffected family members or controls. However, both mutant and wildtype alleles were reduced in mRNA expression, and the authors found no causative mutation for this phenomenon in the ABCA1 gene or its proximal promoter. Albrecht et al. (2005) suggested that a putative second mutation in a trans-acting regulatory gene might be involved in the disorder in this patient.


REFERENCES

  1. Ahmad, S. S., Rawala-Sheikh, R., Ashby, B., Walsh, P. N. Platelet receptor-mediated factor X activation by factor IXa. J. Clin. Invest. 84: 824-828, 1989. [PubMed: 2547839, related citations] [Full Text]

  2. Albrecht, C., McVey, J. H., Elliott, J. I., Sardini, A., Kasza, I., Mumford, A. D., Naoumova, R. P., Tuddenham, E. G. D., Szabo, K., Higgins, C. F. A novel missense mutation in ABCA1 results in altered protein trafficking and reduced phosphatidylserine translocation in a patient with Scott syndrome. Blood 106: 542-549, 2005. [PubMed: 15790791, related citations] [Full Text]

  3. Basse, F., Stout, J. G., Sims, P. J., Wiedmer, T. Isolation of an erythrocyte membrane protein that mediates Ca(2+)-dependent transbilayer movement of phospholipid. J. Biol. Chem. 271: 17205-17210, 1996. [PubMed: 8663431, related citations] [Full Text]

  4. Boisseau, P., Bene, M. C., Besnard, T., Pachchek, S., Giraud, M., Talarmain, P., Robillard, N., Gourlaouen, M. A., Bezieau, S., Fouassier, M. A new mutation of ANO6 in two familial cases of Scott syndrome. Brit. J. Haemat. 180: 750-752, 2018. [PubMed: 27879994, related citations] [Full Text]

  5. Bouchaib, A. E., Balde, M. A., Babahabib, A., Elhassani, M. E. M., Kouach, J. Syndrome de Scott et grossesse: a propos d'un cas. Pan Afr. Med. J. 44: 151, 2023. [PubMed: 37455884, related citations] [Full Text]

  6. Brooks, M. B., Catalfamo, J. L., Brown, H. A., Ivanova, P., Lovaglio, J. A hereditary bleeding disorder of dogs caused by a lack of platelet procoagulant activity. Blood 99: 2434-2441, 2002. [PubMed: 11895776, related citations] [Full Text]

  7. Castoldi, E., Collins, P. W., Williamson, P. L., Bevers, E. M. Compound heterozygosity for 2 novel TMEM16F mutations in a patient with Scott syndrome. Blood 117: 4399-4400, 2011. [PubMed: 21511967, related citations] [Full Text]

  8. Kojima, H., Newton-Nash, D., Weiss, H. J., Zhao, J., Sims, P. J., Wiedmer, T. Production and characterization of transformed B-lymphocytes expressing the membrane defect of Scott syndrome. J. Clin. Invest. 94: 2237-2244, 1994. [PubMed: 7989579, related citations] [Full Text]

  9. Miletich, J. P., Jackson, C. M., Majerus, P. W. Interaction of coagulation factor Xa with human platelets. Proc. Nat. Acad. Sci. 74: 4033-4036, 1977. [PubMed: 333455, related citations] [Full Text]

  10. Miletich, J. P., Jackson, C. M., Majerus, P. W. Properties of the factor Xa binding site on human platelets. J. Biol. Chem. 253: 6908-6916, 1978. [PubMed: 690132, related citations]

  11. Miletich, J. P., Kane, W. H., Hofmann, S. L., Stanford, N., Majerus, P. W. Deficiency of factor Xa--factor Va binding sites on the platelets of a patient with a bleeding disorder. Blood 54: 1015-1022, 1979. [PubMed: 497393, related citations]

  12. Munnix, I. C. A., Harmsma, M., Giddings, J. C., Collins, P. W., Feijge, M. A. H., Comfurius, P., Heemskerk, J. W. M., Bevers, E. M. Store-mediated calcium entry in the regulation of phosphatidylserine exposure in blood cells from Scott patients. Thromb. Haemost. 89: 687-695, 2003. [PubMed: 12669124, related citations]

  13. Parry, D. H., Giddings, J. C., Bloom, A. L. Familial haemostatic defect associated with reduced prothrombin consumption. Brit. J. Haemat. 44: 323-334, 1980. [PubMed: 7378303, related citations] [Full Text]

  14. Robinson, A. J., Aggeler, P. M., McNicol, G. P., Douglas, A. S. An atypical genetic haemorrhagic disease with increased concentration of a natural inhibitor of prothrombin consumption. Brit. J. Haemat. 13: 510-527, 1967. [PubMed: 6029953, related citations] [Full Text]

  15. Rosing, J., Bevers, E. M., Comfurius, P., Hemker, H. C., van Dieijen, G., Weiss, H. J., Zwaal, R. F. A. Impaired factor X and prothrombin activation associated with decreased phospholipid exposure in platelets from a patient with a bleeding disorder. Blood 65: 1557-1561, 1985. [PubMed: 3995186, related citations]

  16. Stout, J. G., Basse, F., Luhm, R. A., Weiss, H. J., Wiedmer, T., Sims, P. J. Scott syndrome erythrocytes contain a membrane protein capable of mediating Ca(2+)-dependent transbilayer migration of membrane phospholipids. J. Clin. Invest. 99: 2232-2238, 1997. [PubMed: 9151796, related citations] [Full Text]

  17. Suzuki, J., Umeda, M., Sims, P. J., Nagata, S. Calcium-dependent phospholipid scrambling by TMEM16F. Nature 468: 834-838, 2010. [PubMed: 21107324, related citations] [Full Text]

  18. Toti, F., Satta, N., Fressinaud, E., Meyer, D., Freyssinet, J.-M. Scott syndrome, characterized by impaired transmembrane migration of procoagulant phosphatidylserine and hemorrhagic complications, is an inherited disorder. Blood 87: 1409-1415, 1996. [PubMed: 8608230, related citations]

  19. Weiss, H. J., Vicic, W. J., Lages, B. A., Rogers, J. Isolated deficiency of platelet procoagulant activity. Am. J. Med. 67: 206-213, 1979. [PubMed: 572637, related citations] [Full Text]

  20. Weiss, H. J. Scott syndrome: a disorder of platelet coagulant activity. Semin. Hemat. 31: 312-319, 1994. [PubMed: 7831576, related citations]


Marla J. F. O'Neill - updated : 10/23/2023
Hilary J. Vernon - updated : 10/18/2023
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Marla J. F. O'Neill - updated : 10/14/2005
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# 262890

SCOTT SYNDROME; SCTS


Alternative titles; symbols

BLEEDING DISORDER, PLATELET-TYPE, 7; BDPLT7
BLEEDING ABNORMALITY DUE TO DEFICIENCY OF PLATELET BINDING OF FACTOR X
PROTHROMBIN CONVERSION DEFECT, FAMILIAL
PROTHROMBIN CONSUMPTION DEFICIENCY
PROTHROMBIN CONSUMPTION INHIBITOR, FAMILIAL


SNOMEDCT: 128098009;   ORPHA: 806;   DO: 0111052;   MONDO: 0009885;  


Phenotype-Gene Relationships

Location Phenotype Phenotype
MIM number
Inheritance Phenotype
mapping key
Gene/Locus Gene/Locus
MIM number
12q12 Scott syndrome 262890 Autosomal recessive 3 ANO6 608663

TEXT

A number sign (#) is used with this entry because of evidence that Scott syndrome (SCTS) is caused by homozygous or compound heterozygous mutation in the TMEM16F gene (ANO6; 608663) on chromosome 12q12.


Description

Scott syndrome (SCTS) is a mild platelet-type bleeding disorder characterized by impaired surface exposure of procoagulant phosphatidylserine (PS) on platelets and other blood cells, following activation with Ca(2+)-elevating agents (Munnix et al., 2003).

For a discussion of genetic heterogeneity of platelet-type bleeding disorder (BDPLT), see 231200.


Clinical Features

In 4 generations of a family (with 1 instance of male-to-male transmission), Robinson et al. (1967) described a mild bleeding disorder with no spontaneous hemorrhage. Analysis of blood coagulation in 2 generations revealed normal values for all clotting factors and other hemostatic systems except prothrombin consumption and thromboplastin inactivation. Robinson et al. (1967) demonstrated the presence of what they termed an 'inactivator' of active factor X (F10; 613872) in the plasma of these patients which accelerated the decay of blood thromboplastin. The inhibitor resembled that commonly observed in systemic lupus erythematosus; a similar agent was found in normal plasma but in much smaller amounts.

Parry et al. (1980) studied 10 individuals from 3 unrelated Welsh families who had reduced prothrombin conversion as shown by a grossly abnormal prothrombin consumption index (PCI). Male-to-male transmission was reported. All known plasma coagulation factors were present in adequate concentrations; some affected persons had mild postoperative or postpartum bleeding but none suffered spontaneous bleeding. In therapeutic trials both plasma and platelet transfusions were needed to correct the abnormality. This finding, together with in vitro and other in vivo studies, suggested to Parry et al. (1980) that the abnormality was associated with an inhibitor of the interaction between plasma and phospholipid during blood coagulation. Parry et al. (1980) considered the abnormality similar but not identical to that in several members of the family reported by Robinson et al. (1967).

Kojima et al. (1994) demonstrated that the coagulant nonresponder phenotype observed in platelets and erythrocytes in Scott syndrome is expressed by all of the EBV-transformed lymphoblasts derived from the B cells of the patient, and that the unique phenotype of the defective cells can be isolated by single cell cloning and propagated in culture through many generations. The continuous expression of the aberrant phenotype through in vitro culture confirmed that the Scott syndrome defect represents a gene deletion or mutation that is passed to daughter cells through mitosis. Furthermore, they demonstrated by heterokaryon hybridoma fusion that the abnormal Scott phenotype can be corrected by fusion with a cell exhibiting the normal coagulant-responder phenotype, and that the normal phenotype is sustained when these hybridomas are subsequently propagated through many generations. Taken together with the results of previous studies, these data suggested that the cellular defect in Scott syndrome reflects a mutation or deletion of a gene required for normal Ca(2+)-dependent transbilayer migration of phosphatidylserine to the plasma membrane surface and that this defect is shared among the blood cells of lymphoid, megakaryocytic, and erythroid lineages.

Toti et al. (1996) characterized a familial instance of Scott syndrome and confirmed that it is a genetic disorder affecting the outward transmembrane migration of phosphatidylserine. Low prothrombin consumption in the serum of the proposita, a 71-year-old woman, and 2 of her children was the sole abnormal hemostasis parameter. The degree of exposure of procoagulant phospholipids, chiefly phosphatidylserine, was reduced in stimulated platelets, erythrocytes, and EBV-infected B lymphocytes, indicating that multiple hematologic lineages are affected in this disorder. The data were considered compatible with homozygous status of the proposita and heterozygous status of her children. Toti et al. (1996) concluded that Scott syndrome is transmitted as an autosomal recessive trait, reflecting the deletion or mutation of a putative outward phosphatidylserine translocase.

Boisseau et al. (2018) reported 2 sibs with Scott syndrome who were identified due to bleeding during surgery. Ionophore activation of platelets from the patients demonstrated low phosphatidylserine expression.

Bouchaib et al. (2023) reported a 36-year-old Moroccan woman, born of consanguineous parents, who developed a palatal hematoma after dental extraction, had an episode of uterine bleeding, and experienced a miscarriage at 2 months in a pregnancy that was complicated by prolonged uterine bleeding. Laboratory evaluation after the miscarriage revealed a defect in phospholipid scramblase, and the diagnosis of Scott syndrome was confirmed by flow cytometry showing absent or reduced phosphatidylserine on the platelet surface. A second pregnancy 5 years later was uneventful; with the support of preventive measures during delivery, including intravenous antifibrinolytic agents as well as transfusions of platelets and red blood cells, she gave birth to a healthy boy. The authors stated that in published reports of 5 patients with Scott syndrome who had given birth, all experienced postpartum hemorrhage requiring hysterectomy for hemostasis, and there were 2 maternal deaths. The authors recommended that, given the high risk for postpartum hemorrhage, a multidisciplinary team and preventive measures should be available for pregnancy and delivery in women with Scott syndrome.

Reviews

See review of Scott syndrome by Weiss (1994).


Biochemical Features

Miletich et al. (1977, 1978) demonstrated that each platelet has about 200 binding sites with high affinity specifically for activated factor X (factor Xa). Bound factor Xa is 300,000 times more active than free factor Xa in generating thrombin from prothrombin and is protected from inactivation by antithrombin III. Factor V (612309) is also essential for the binding process. The important physiologic role of the platelet receptor for factor X was indicated by the studies (Miletich et al., 1979) of a woman with a hemorrhagic diathesis due to deficiency of the platelet receptor who was first reported by Weiss et al. (1979). Receptors in the parents were normal; however, Miletich et al. (1979) did not exclude autosomal recessive inheritance. Since the patient's value for factor X binding was 25% of normal, the heterozygous state might be characterized by values 75% of normal, which would be indistinguishable from the normal range. Rosing et al. (1985) confirmed the deficiency in capacity to promote prothrombin activation in this patient and demonstrated a deficiency in the ability to promote factor X activation as well. Rosing et al. (1985) also showed that the platelets were defective in the capacity to expose phosphatidylserine at the outer surface of stimulated platelets. In further studies of the same patient, Ahmad et al. (1989) described findings suggesting impairment of factor VIIIa binding.

Phospholipid scramblase (see 604170) is a plasma membrane protein purified by Basse et al. (1996) that mediates accelerated transbilayer migration of phospholipids upon binding calcium ions, facilitating rapid mobilization of phosphatidylserine to the cell surface upon elevation of internal Ca(2+). In patients with Scott syndrome, circulating blood cells show decreased cell surface exposure of phosphatidylserine at elevated cytosolic levels of calcium ion, implying an underlying defect or deficiency of phospholipid scramblase. To gain insight into the molecular basis of Scott syndrome, Stout et al. (1997) compared PL scramblase in Scott erythrocyte membranes to those of normal controls. Whereas membranes of Scott cells were unresponsive to Ca(2+)-induced activation of PL scramblase at neutral pH, apparently normal PL scramblase activity was induced at pH less than 6.0. After extraction with octylglucoside, a membrane protein was isolated from the Scott cells that exhibited normal PL scramblase activity when reconstituted in vesicles with exogenous PLs. Like PL scramblase from normal red cells, PL scramblase from Scott red cells was maximally activated by addition of calcium ion (at pH 7.4) or by acidification to pH less than 6.0, and similar apparent affinities for calcium ion and rates of transbilayer transfer of PLs were observed. Stout et al. (1997) suggested that the defect in Scott syndrome is related to an altered interaction of calcium ion with PL scramblase on the endofacial surface of the cell membrane, due either to an intrinsic constraint upon the protein preventing interaction with calcium ion in situ, or to an unidentified inhibitor or cofactor in the Scott cell that is dissociated by detergent.

Munnix et al. (2003) analyzed the relationship between Ca(2+) flux and phosphatidylserine exposure in platelets and B lymphocytes derived from the original Scott syndrome patient (Weiss et al., 1979), a patient from one of the Welsh families reported by Parry et al. (1980), and 2 controls. The 34-year-old Welsh woman, who had a history of excessive bleeding after dental extractions since childhood, suffered life-threatening postpartum hemorrhage after an uncomplicated forceps delivery. Munnix et al. (2003) found that although she had normal levels of coagulation factors and normal platelet aggregation, her collagen-activated platelets showed only 52% of the prothrombinase activity of a control and had markedly reduced phosphatidylserine exposure, confirming the phenotype of Scott syndrome. Ca(2+) entry into platelets and lymphoblasts from both patients was normal, and elevated intracellular free Ca(2+) concentrations resulting from store-mediated Ca(2+) entry was not sufficient to trigger phosphatidylserine exposure.


Inheritance

The transmission pattern of SCTS in the family reported by Suzuki et al. (2010) was consistent with autosomal recessive inheritance.


Molecular Genetics

Suzuki et al. (2010) identified homozygosity for a splice site mutation in the TMEM16F gene (608663.0001) in the patient with Scott syndrome reported by Weiss et al. (1979) and Kojima et al. (1994).

In 2 sibs with Scott syndrome, Boisseau et al. (2018) identified compound heterozygous mutations in the ANO6 gene (608663.0002-608663.0003). The mutations were identified by Sanger sequencing of the ANO6 gene and copy number analysis from next-generation sequencing data.

By sequencing of the ANO6 gene in a Welsh woman with Scott syndrome, Castoldi et al. (2011) identified compound heterozygous mutations (608663.0004-608773.0005).

By high-throughput sequencing in a 36-year-old Moroccan woman with Scott syndrome, born of consanguineous parents, Bouchaib et al. (2023) identified homozygosity for a nonsense mutation in the ANO6 gene (R440X; 608663.0006). The authors noted that Scott syndrome is likely underdiagnosed, given the relatively benign clinical presentation of most patients.


Nomenclature

The bleeding disorder in the patient studied by Weiss et al. (1979) was referred to as Scott syndrome, presumably on the basis of the patient's surname (Ahmad et al., 1989).


Animal Model

Brooks et al. (2002) discovered a novel canine hereditary bleeding disorder with the characteristic features of Scott syndrome. Affected dogs were from a single, inbred colony and experienced clinical signs of epistaxis, hyphema (hemorrhage into the anterior chamber of the eye), intramuscular hematoma, and prolonged bleeding with cutaneous bruising after surgery. The hemostatic abnormalities were restricted to tests of platelet procoagulant activity, whereas platelet count, platelet morphology under light microscopy, bleeding time, clot retraction, and platelet aggregation and secretion in response to thrombin, collagen, and adenosine diphosphate stimulation were all within normal limits. Washed platelets from the affected dogs demonstrated approximately twice normal clotting times in a platelet factor-3 availability assay and, in a prothrombinase assay, generated only background levels of thrombin in response to calcium ionophore, thrombin, or combined thrombin plus collagen stimulation. These studies indicated recessive inheritance.


History

In a patient with Scott syndrome, Albrecht et al. (2005) identified a heterozygous missense mutation (arg1925 to gln) in the ABCA1 gene (600046), which was not found in unaffected family members or controls. However, both mutant and wildtype alleles were reduced in mRNA expression, and the authors found no causative mutation for this phenomenon in the ABCA1 gene or its proximal promoter. Albrecht et al. (2005) suggested that a putative second mutation in a trans-acting regulatory gene might be involved in the disorder in this patient.


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Contributors:
Marla J. F. O'Neill - updated : 10/23/2023
Hilary J. Vernon - updated : 10/18/2023
Ada Hamosh - updated : 1/31/2011
Marla J. F. O'Neill - updated : 10/14/2005
Marla J. F. O'Neill - updated : 10/12/2005
Victor A. McKusick - updated : 5/20/2002
Victor A. McKusick - updated : 5/27/1997

Creation Date:
Victor A. McKusick : 6/25/1986

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