Abstract
The heritable hypermobility syndromes are a group of disorders in which joint laxity is a prominent feature. In some of these conditions the loosejointedness predisposes to a wide variety of articular complications and, despite their rarity, they are therefore of considerable rheumatological importance.
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Ehlers-Danlos Syndrome
Arneson MA, Hammerschmidt DE, Furcht LT, King RA (1980) A new form of Ehlers-Danlos syndrome: fibronectin corrects defective platelet function. JAMA 224: 144–147
Atalla A, Page I (1988) Ehlers-Danlos syndrome type III in pregnancy. Obstet Gynecol 71: 508–509
Barabas AP (1967) Heterogeneity of the Ehlers-Danlos syndrome: Description of three clinical types and a hypothesis to explain the basic defect(s). Br Med J 2: 612–616
Beasley RP, Cohen MM (1979) A new presumably autosomal recessive form of the Ehlers-Danlos syndrome, Clin Genet 16: 19–24
Behrens-Baumann W, Gebauer HJ, Langenbeck U (1977) Syndrome of blue sclerae and keratoglobus (ocular type of Ehlers-Danlos syndrome). Arch Klin Opthalmol 204: 235–246
Beighton P (1968a) X-linked recessive inheritance in the Ehlers-Danlos syndrome, Br Med J 3: 409–414
Beighton P (1968b) Lethal complications of the Ehlers-Danlos syndrome. Br Med J 3: 656–660
Beighton P (1970a) The Ehlers-Danlos syndrome, William Heinemann Medical Books, London Beighton P (1970b) Serious ophthalmological complications in the Ehlers-Danlos syndrome. Br J Ophthalmol 54: 263–269
Beighton P, Curtis D (1985) X-linked Ehlers-Danlos syndrome type V: the next generation. Clin Genet 27: 472–478
Beighton P, Horan F (1969) Orthopaedic aspects of the Ehlers-Danlos syndrome. J Bone Joint Surg [BR] 51: 414–449
Beighton P, Murdoch JL, Votteler T (1969a) Gastrointestinal complications of the Ehlers-Danlos syndrome. Gut 10: 1004–1008
Beighton P, Price A, Lord A, Dickson E (1969b) Variants of the Ehlers-Danlos syndrome. Clinical, biochemical, haematological and chromosomal features of 100 patients. Ann Rheum Dis 28: 228–235
Bilkey WJ, Baxter TL, Kottke FJ, Mundale MO (1981) Muscle formation in Ehlers-Danlos syndrome. Arch Phys Med Rehabil 62: 444–448
Byers PH, Holbrook KA, McGillivray B, MacLeod PM, Lowry RB (1979) Clinical and ultrastructural heterogeneity of type IV Ehlers-Danlos syndrome. Hum Genet 47: 141–150
Cabeen WR, Reza MJ, Kovick RB, Stern MS (1977) Mitral valve prolapse and conduction defects in Ehlers-Danlos syndrome. Arch Intern Med 137: 1227–1231
Chouza C, Caamano JL, De Medina O et al. (1984) Familial spastic ataxia associated with Ehlers-Danlos syndrome with platelet dysfunction. Can J Neurol Sci 11: 541–549
Cole WG, Chan D, Chambers GW, Walker ID, Bateman JF (1986) Deletion of 24 amino acids from the prol(I) chain of type I procollagen in a patient with Ehlers-Danlos syndrome type VII. J Biol Chem 261: 5496–5503
Danlos M (1908) Un cas de cutis Laxa avec tumeurs par contusion chronique des coudes et des genoux (Xanthome juvenile pseudodiabetique de M M Hallopeau et Mace de Lepinay). Bull Soc Franc Derm Syph 19: 70–72
Denko CW (1978) Chernogubov’s syndrome: a translation of the first modern case report of the Ehlers-Danlos syndrome, J Rheumatol 5: 347–352
Di Ferrante N, Leachman RD, Angelini P, Donnelly PV, Francis G, Almazan A, Segni G (1975) Lysyl oxidase deficiency in Ehlers-Danlos syndrome type V. Connect Tissue Res 3: 49–53
Ehlers E (1901) Cutis Laxa, Niegung zu Haemorrhagien in der Haut, Lockerung Mehrer Artikulationen. Derm Z 8: 173–175
Estes JW (1968) Platelet size and function in the heritable disorders of connective tissue. Ann Intern Med 68: 1237–1249
Eyre DR, Shapiro FD, Aldridge GH (1985) A heterozygous collagen defect in a variant of the Ehlers-Danlos syndrome type VII. J Biol Chem 260: 11,322–11, 329
Goodman RM, Allison ML, (1969) Chronic temporomandibular joint subluxation in EhlersDanlos syndrome: report of case. J Oral Surg 27: 659–661
Hernandez A, Aguirre-Negrete MG, Ramirez-Soltero S, Gonzalez-Mendoza A, Martinez y Martinez R, Velazquez-Cabrera A, Cantu JM (1979) A distinct variant of the Ehlers-Danlos syndrome. Clin Genet 16: 335–339
Hernandez A, Aguirre-Negrete MG, Liparoli JC, Canto JM (1981) Third case of a distinct variant of the Ehlers-Danlos syndrome ( EDS ). Clin Genet 20: 222–224
Hernandez A, Aguirre-Negrete MG, Gonzales-Flores S et al. (1986) Ehlers-Danlos features with progeroid facies and mild mental retardation. Further delineation of the syndrome. Clin Genet 30: 456–461
Hollister DW (1982) Clinical features of Ehlers-Danlos syndrome type VIII and IX. In: Akeson WH (ed) Symposium on heritable disorders of connective tissue. CV Mosby, St Louis, pp 102–113
Hulme JR, Wilmshurst CC (1976) Acute appendicitis in the Ehlers-Danlos syndrome. Am J Surg 132: 103–104
Kashiwagi H, Riddle JM, Abraham JP, Frame B (1965) Functional and ultrastructural abnormalities of platelets in Ehlers-Danlos syndrome. Ann Intern Med 63: 249–254
Krane SM (1982) Hydroxylysine-deficient collagen disease. A form of Ehlers-Danlos syndrome type VI. In: Akeson WH (ed) Symposium on heritable disorders of connective tissue. CV Mosby, St Louis, pp 61–81
Leier CV, Call TD, Fulkerson PK, Wooley CF (1980) The spectrum of cardiac defects in the Ehlers-Danlos syndrome, types I and III. Ann Intern Med 92: 171–178
Lichtenstein JR, Martin GR, Kohn LD, Byers PH, McKusick VA (1974) Defect in conversion of procollagen in a form of Ehlers-Danlos syndrome. Science 182: 298–300
Mabille JP, Castera D, Chapuis JL, Lambert D, Chapelion (1972) Un cas de syndrome d’Ehlers-Danlos, avec acro-osteolyse. Ann Radiol 15: 781–786
McFarland W, Fuller DE (1964) Mortality in Ehlers-Danlos syndrome due to spontaneous rupture of large arteries. N Eng J Med 271: 1309–1312
McKusick VA (1972) Heritable disorders of connective tissue, 4th edn. CV Mosby Co, St Louis Baltimore
McKusick VA (1978) Mendelian inheritance in man, 5th edn. John S Hopkins University Press, Baltimore
Nelson DL, King RA (1981) Ehlers-Danlos syndrome type VIII. J Am Acad Dermatol 5: 297–303
Onel D, Ulutin SB, Ulutin ON (1973) Platelet defect in a case of Ehlers-Danlos syndrome. Acta Haematol 50: 238–244
Osborn TG, Lichtenstein JR, Moore TL, Weiss T, Zuckner J (1981) Ehlers-Danlos syndrome presenting as rheumatic manifestations in the child, J Rheumatol 8: 79–85
Pinnell SR, Krane SM, Kenzora JE, Glimcher A (1972) A heritable disorder of connective tissue: hydroxylysine deficient collagen disease. N Engl J Med 286: 1013–1020
Pope FM, Martin GR, Lichenstein JR, Penttinen R, Gerson B, Rowe DW (1975) Patients with Ehlers-Danlos syndrome type IV lack type III collagen. Proc Natl Acad Sci USA 72: 1314–1316
Pope FM, Martin GR, McKusick VA (1977) Inheritance of Ehlers-Danlos type IV syndrome. J Med Genet 14: 200–204
Pope FM, Nicholls AC, Jones PM, Wells RS, Lawrence D (1980) EDS IV (acrogeria): new autosomal dominant and recessive types. J R Soc Med 73: 180–186
Pyeritz RE, Stolle CA, Parfrey NA, Myers JC (1984) Ehlers-Danlos syndrome IV due to a novel defect in type III procollagen. Am J Med Genet 19: 607–622
Rao AA (1979) Ehlers-Danlos syndrome with monostotic fibrous dysplasia. J Postgrad Med 25: 186–188
Ronchese F (1936) Dermatorrhexis with dermatochalasis and arthrochalasis (the so-called Ehlers-Danlos syndrome). Am J Dis Child 51: 1403–1406
Siegel RC, Black CM. Bailey AJ (1979) Cross-linking of collagen in the X-linked Ehlers-Danlos type V. Biochem Biophys Res Commun 88: 287
Stewart RE, Hollister DW, Rimoin DL (1977) A new variant of Ehlers-Danlos syndrome: an autosomal dominant disorder of fragile skin, abnormal scarring and generalised periodontitis. Birth Defects: XIII 85–93
Steinmann B, Tuderman L, Peltonen L, Martin GR, McKusick VA, Prockop DJ (1980) Evidence for a structural mutation of procollagen type I in a patient with Ehlers-Danlos syndrome type VII. J Biol Chem 255: 8887–8893
Stolle CA, Pyeritz RE, Myers JC, Prockop DJ (1985) Synthesis of an altered type III procollagen in a patient with type IV Ehlers-Danlos syndrome. J Biol Chem 260: 1037–1944
Sulica VI, Cooper PH, Pope FM, Hambrick GW, Garson BM, McKusick VA (1979) Cutaneous histologic features in Ehlers-Danlos syndrome: study of 21 patients. Arch Dermatol 115: 40–42
Viljoen D, Goldblatt J, Thompson D, Beighton P (1987) Ehlers-Danlos syndrome: yet another type? Clin Genet 32: 196–201
Familial Articular Hypermobility Syndromes
Beighton P (1970) The Ehlers-Danlos syndrome. William Heinemann Medical Books, London.
Beighton P, Horan FT (1970) Dominant inheritance in familial generalised articular hypermobility. J Bone Joint Surg [BR] 52: 145–147
Bjerkreim I, van der Hagen CB (1974) Congenital dislocation of the hip in Norway. Clin Genet 5: 433–448
Carter C, Sweetnam R (1958) Familial joint laxity and recurrent dislocations of the patella. J Bone Joint Surg [BR] 40: 664–667
Carter C, Sweetnam R (1960) Recurrent dislocation of the patella and of the shoulder, their association with familial joint laxity. J Bone Joint Surg [BR] 42: 721–727
Carter C, Wilkinson J (1964) Persistent joint laxity and congenital dislocation of the hip. J Bone Joint Surg [BR] 46: 40–45
Fredensborg N (1978) Unilateral joint laxity in unilateral congenital dislocation of the hip. Int Orthop 2: 177–178
Grahame R, Edwards JC, Pitcher D, Gabell A, Harvey W (1981) A clinical and echocardiographic study of patients with the hypermobility syndrome. Ann Rheum Dis 40: 541–546
Hass J, Hass R (1958), Arthrochalasis multiplex congenita. J Bone Joint Surg [Am] 40: 663–674
Horan FT, Beighton P (1973) Recessive inheritance of generalized joint hypermobility. Rheumatol Rehabil 12: 47–49
Horton WA, Collins DL, DeSmet AA, Kennedy JA, Schimke RN (1980) Familial joint instability syndrome. Am J Med Genet 6: 221–228
Key JA (1927) Hypermobility of joints as a sex-linked hereditary characteristic. JAMA 88: 1710–1712
Shapiro SD, Jorgenson RJ, Salinas CF (1976) Recurrent dislocation of the patella versus generalized joint laxity. The National Foundation. Birth Defects XII: 287–291
Steinmann B, Tuderman L, Martin GR, Prockop DJ (1979) Evidence for a structural mutation of procollagen in a patient with Ehlers-Danlos syndrome type VII. Eur J Pediat 130: 203–205
Sturkie PD (1941) Hypermobile joints in all descendants for two generations. J Hered 32: 232–234
Whitney LF (1932) Inheritance of double-jointedness of the thumb. J Hered 23: 425–426
Wynne-Davis R (1970a) Acetabular dysplasia and familial joint laxity, two etiologic factors in congenital dislocation of the hip. J Bone Joint Surg [BR] 52: 704–716
Wynne-Davis R (1970b) A familial study of neonatal and late-diagnosis congenital dislocation of the hip. J Med Genet 7: 315–333
Miscellaneous Joint Laxity Syndromes
Aarskog D (1970) A familial syndrome of short stature associated with facial dysplasia and genital anomalies. J Pediatr 77: 856–861
Balestrazzi P, Corrini L, Villani G, Bolla MP, Casa F, Bernasconi S (1980) The Cohen syndrome: clinical and endocrinological studies of two new cases. J Med Genet 17: 430–432
Beals RK (1969) Hypochondroplasia. J Bone Joint Surg [Am] 51: 728–739
Beighton P (1974) Autosomal recessive inheritance in the mesomelic dwarfism of Campailla and Martinelli. Clin Genet 5: 363–367
Beighton P (1988) Inherited disorders of the skeleton. Churchill Livingstone, Edinburgh, London, New York
Beighton P, Craig J (1973) Atlanto-axial dislocation in the Morquio syndrome. J Bone Joint Surg [BR] 55: 478–480
Beighton PH, Kozlowski K (1980) Spondo-epi-metaphyseal dyplasia with joint laxity and severe progressive kyphoscoliosis. Skeletal Radiol 5: 205–317
Beighton P, Kozlowski K, Gericke G, Wallis G, Grobler L (1983) Spondylo-epimetaphyseal dysplasia with joint laxity and severe, progressive kyphoscoliosis. S Afri Med J 64: 772–775
Beighton P, Gericke G, Kozlowski K, Grobler L (1984) The manifestations and natural history of spondyloepimetaphyseal dysplasia with joint laxity. Clin Genet 26: 308–317
Benson DR, Newman DC (1981) The spine and surgical treatment in osteogenesis imperfecta. Clin Orthop 159: 147–153
Bianchine JW, Murdoch JL (1969) Juvenile osteoporosis (?) in a boy with bilateral enucleation of the eyes for pseudoglioma,. The clinical delineation of birth defects. IV. Skeletal dysplasias. Birth Defects V: 225–226
Biering A, Iverson T (1955) Osteogenesis imperfecta associated with Ehlers-Danlos syndrome. Acta Paediatr Scand 44: 279–283
Biglan AW, Brown SI, Johnson BL (1977) Keratoglobus and blue sclerae. Am J Ophthalmol 83: 225–233
Birkenstock WE, Louw JH, Maze A, Sladen RN (1973) Combined Ehlers-Danlos and Marfan’s syndromes with a case report. SA Med J 47: 2097–2102
Brown DM, Bradford DS, Gorlin RJ, Desnick RJ, Langer LO Jr, Jowsey J, Sauk JJ Jr (1976) The acro-osteolysis syndrome: morphologic and biochemical studies. J Pediatr 88: 573–580
Byers PH, Narayanan AS, Bornstein P, Hall JG (1976) An X-linked form of cutis laxa due to deficiency of lysyloxidase. Birth defects XII: 293–298
Carey JC, Bryan DH (1978) Confirmation of the Cohen syndrome. J Pediatr 93: 239–244
Coffins GS, Siris E (1970) Mental retardation with absent fifth fingernail and terminal phalanx. Am J Dis Child 119: 433–439
Daneshwar A, Tavakol D, Nozarian J (1979) Marfanoid hypermobility syndrome associated with coarctation of the aorta. Br Heart J 41 (5): 621–623
Debré R, Marie J, Seringe P (1937) ‘Curis Laxa’ avec dystrophies osseuses. Bull Mem Soc Med Hosp Paris 53: 1038–1039
Desbuquois G, Grenier B, Michel J, Rossignot C (1966) Nanisme chondrodystrophique avec ossification anarchique et polymalformations chez deux soeurs. Arch Fr Pediatr 23: 573–587
Ghadimi H, Binnington VI, Pecora P (1965) Hyperlysinemia associated with mental retardation. New Engl J Med 273: 723–729
Goldblatt J, Wallis C, Viljoen D (1987) A new hypospadias-mental retardation syndrome in three brothers. Am J Dis Child 141: 1168–1169
Goldblatt J, Wallis C, Viljoen D, Beighton P (1988) Cutis laxa, retarded development and joint hyper/nobility syndrome. Dysmorph Clin Genet 1: 142–144
Gorlin RJ, Mirkin BL (1972) Multiple mucosal neuromas, phaeochromocytama, medullary carcinoma of the thyroid and marfanoid body build with muscle wasting. Syndrome of hyperplasia and neoplasia of neural crest derivatives. A unitarian concept. Z Kinderheilk 113: 313–321
Greenberg AD (1968) Atlantoaxial dislocation. Brain 91: 655–684
Greenfield G, Romano A, Stein R, Goodman RM (1973) Blue sclerae and keratoconus: key features of a district heritable disorder of connective tissue. Clin Genet 4: 8–16
Guizar-Vazquez J, Sanchez G, Manzano C (1980) Peculiar face, pectus carinatum and joint laxity in brother and sister. Clin Genet 18 /4: 280–283
Hall BD, Langer LO, Giedion A, Smith DW, Cohen MM, Beals RK, Bradner M (1974) Langer-Giedion syndrome. Birth Defects X: 147–164
Hall JG (1975) Pseudoachondroplasia. Birth Defects XI: 187–202
Harris R, Cullen CH (1971) Autosomal dominant inheritance in Larsen’s syndrome. Clin Genet 2: 87–90
Heselson NG, Cremin BJ, Beighton P (1977) Pseudoachondroplasia, a report of 13 cases. Br J Radiol 50: 473–482
Holtgrewe JL, Kalen V (1986) Orthopaedic manifestations of the Lowe (oculocerebrorenal) syndrome. J Pediatr Orthop 6: 165–171
Hunter AGW, Thompson DR, Reed MH, Macrodimitris AG (1979) Night blindness, characteristic facies, and skeletal abnormalities in two brothers. J Med Genet 16: 309–313
Kiel EA, Frias JL, Victoria BE (1983) Cardiovascular manifestations in the Larsen syndrome. Pediatrics 71: 942–946
Kozlowski K (1976) Pseudoachondroplastic dysplasia (Maroteaux-Lamy). Austral Radiol 20: 255–269
Kozlowski J, Beighton P (1984) Radiographic features of spondyloepimetaphyseal dysplasia with joint laxity and progressive kyphoscoliosis. Fortschr Geb Rontgenstr Nuklearmed Erganzungsband 141: 337–341
Kozlowski K, Harrington G, Barylak A, Bartoszewica B (1977) Multiple exostoses-mental retardation syndrome (Ale-Calo or M.E.M.R. syndrome): description of two childhood cases. Cln Pediatr 11: 219–224
Larsen LJ, Schottstaedt ER, Bost FC (1950) Multiple congenital dislocations associated with characteristic facial abnormality. J Pediatr 37: 574–581
Latta RJ, Graham CB, Aase J, Scham SM, Smith DW (1971) Larsen’s syndrome: a skeletal dysplasia with multiple joint dislocations and unusual facies. J Pediatr 78: 291–298
Livingstone B, Hirst P: (1984) Orthopedic disorders in school children with Down’s syndrome, with special reference to the incidence of joint laxity. Clin Orthop 207: 74–76
Lowry RB, Wood BJ, Birkbeck JA, Padwick PH (1970) Cartilage-hair hypoplasia. A rare and recessive cause of dwarfism. Clin Pediatr 9: 44–46
Lucaya J, Garcia-Conesa JA, Bosch-Banyeras JM, Pons-Peradejordi G (1981) The Coffin-Siris syndrome. A report of four cases and review of the literature. Pediatr Radio111: 35–38
Maroteaux P (1975) Heterogeneity of Larsen’s syndrome. Arch Fr Pediatr 32: 597–603
McKusick VA (1972) Heritable disorders of connective tissue, 4th edn. CV Mosby, St Louis
McKusick VA, Egeland JA, Eldridge R, Krusen DE (1964) Dwarfism in the Amish. The Ellis-van Creveld syndrome. Bull Johns Hopkins Hosp 115: 306–336
McKusick VA, Eldridge R, Hostetler JA, Egeland JA, Ruangwit U (1965) Dwarfism in the Amish. II. Cartilage-hair hypoplasia. Bull Johns Hopkins Hosp 116: 285–326
Meigel WN, Muller PK, Pontz BF, Sorrensen N, Spranger J (1974) A constitutional disorder of connective tissue suggesting a defect in collagen synthesis. Klin Wochenschr 52: 906–910
Mirovsky Y, Halperin N, Capeliovitch L, Tieder M (1984) Multiple exostoses-mental retardation syndrome. Clin Orthop 185: 72–76
Neuhauser G, Kaveggia EG, Opitz JM (1976) Autosomal recessive syndrome of pseudogliomatous blindness, osteoporosis and mild mental retardation. Clin Genet 9: 324–332
Oberklaid F, Danks DM (1975) The Opitz trigonocephaly syndrome: a case report. Am J Dis Child 129: 1348–1349
Opitz JM, Kaveggia EG (1974) The FG syndrome. An X-linked recessive syndrome of multiple congenital anomalies and mental retardation. Z Kinderheilk 117: 1–18
Opitz JM, Johnson RC, McCreadie SR, Smith DW (1969) The C syndrome of multiple congenital anomalies. The clinical delineation of birth defects. II. Malformation syndromes. Birth Defects V: 161–166
Riccardi VM, Hassler E, Lubinsky MS (1977) The FG syndrome: further characterization, report of a third family, and of a sporadic case. Am J Med Genet 1: 47–58
Robertson FW (1975) Keratoconus and the Ehlers-Danlos syndrome; a new aspect of keratoconus. Med J Aust 1 (18): 571–573
Robertson FW, Kozlowski K, Middleton RW (1975) Larsen’s syndrome. Three cases with multiple congenital joint dislocations and distinctive facies. Clin Genet 14: 53–660
Saltzman CL, Herzenberg JE, Phillips WA, Hensinger RN, Hopwood NJ (1988) Thick lips, bumpy tongue and slipped capital femoral epiphysis; a deadly combination. J Pediatr Orthop 8: 219–222
Schimke RN, Hartmann WH, Prout TE, Rimoin DL (1968) Phaechromocytoma, medullary thyroid carcinoma and multiple neuromas. New Engl J Med 279: 1–7
Smith TH, Holland MG, Woody NC (1971) Ocular manifestations of familial hyperlysinemia? Trans Am Acad Ophthalmol Otolaryngol 75: 355–360
Spranger J, Langer LO (1970) Spondyloepiphyseal dysplasia congenita. Radiology 94: 313–322
Stanley D, Seymour N (1985) The Larsen syndrome occurring in four generations of one family. Int Orthop 8: 267–272
Stiscuiglio P, Sebastio G, Andria G (1983) Severe cardiac anomalies in sibs with Larsen syndrome. J Med Genet 20: 422–424
Sugarman GI, Rimoin DL, Lachman RS (1973) The facial-digital-genital ( Aarskog) syndrome. Am J Dis Child 126: 248–252
Teebi AS, Al Awadi SA, Marafie MJ, Bushnaq RA, Satyanath S (1988) Osteoporosispseudoglioma syndrome with congenital heart disease: a new association. J Med Genet 25: 32–36
Walker BA, Beighton PH, Murdoch JL (1969) The marfanoid hypermobility syndrome. Ann Intern Med 71: 349–352
Weil UH (1981) Osteogenesis imperfecta. Clin Orthop 159: 6–10
Weleber RG, Beals RK (1976) Hadju-Cheney syndrome - report of 2 cases and review of literature. J Pediatr 88: 243–249
Yancey CL, Zmijewski C, Athreya BH, Doughty RA (1984) Arthropathy of Down’s syndrome. Arthritis Rheumatol 27: 929–934
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Beighton, P., Grahame, R., Bird, H. (1989). Heritable Hypermobility Syndromes. In: Grahame, R. (eds) Hypermobility of Joints. Springer, London. https://doi.org/10.1007/978-1-4471-3900-3_10
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