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Volumn 93, Issue 7-12, 2000, Pages 1197-1200

Marfanoid Habitus, Dysmorphic Features, and Web Neck

Author keywords

[No Author keywords available]

Indexed keywords

ADULT; ARTICLE; BONE DYSPLASIA; CASE REPORT; CONGENITAL HEART MALFORMATION; CRANIOFACIAL MALFORMATION; DIFFERENTIAL DIAGNOSIS; HUMAN; MALE; MARFAN SYNDROME; MENTAL DEFICIENCY; MULTIPLE MALFORMATION SYNDROME; PATHOPHYSIOLOGY;

EID: 0034564934     PISSN: 00384348     EISSN: None     Source Type: Journal    
DOI: 10.1097/00007611-200012000-00011     Document Type: Article
Times cited : (4)

References (12)
  • 1
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    • De Paepe, A.1    Devereux, R.B.2    Dietz, H.C.3
  • 2
    • 0032546209 scopus 로고    scopus 로고
    • Shprintzen-Goldberg syndrome: A clinical analysis
    • Greally MT, Carey JC, Milewicz DM, et al: Shprintzen-Goldberg syndrome: a clinical analysis. Am J Med Genet 1998; 76:202-212
    • (1998) Am J Med Genet , vol.76 , pp. 202-212
    • Greally, M.T.1    Carey, J.C.2    Milewicz, D.M.3
  • 3
    • 0030020322 scopus 로고    scopus 로고
    • Mutation in fibrillin-1 and the Marfanoid-craniosynostosis (Shprintzen-Goldberg) syndrome
    • Sood S, Eldadah ZA, Krause WL, et al: Mutation in fibrillin-1 and the Marfanoid-craniosynostosis (Shprintzen-Goldberg) syndrome. Nat Genet 1996; 12:209-211
    • (1996) Nat Genet , vol.12 , pp. 209-211
    • Sood, S.1    Eldadah, Z.A.2    Krause, W.L.3
  • 4
    • 0029016233 scopus 로고
    • Patient with craniosynostosis and marfanoid phenotype (Shprintzen-Goldberg syndrome) and cloverleaf skull
    • Saal HM, Bulas DI, Allen JF, et al: Patient with craniosynostosis and marfanoid phenotype (Shprintzen-Goldberg syndrome) and cloverleaf skull. Am J Med Genet 1995; 57:573-578
    • (1995) Am J Med Genet , vol.57 , pp. 573-578
    • Saal, H.M.1    Bulas, D.I.2    Allen, J.F.3
  • 5
    • 0015322684 scopus 로고
    • "New" syndrome of congenital contractural arachnodactyly originally described by Marfan in 1896
    • Hecht F, Beals RK: "New" syndrome of congenital contractural arachnodactyly originally described by Marfan in 1896. Pediatrics 1971; 49:574-579
    • (1971) Pediatrics , vol.49 , pp. 574-579
    • Hecht, F.1    Beals, R.K.2
  • 6
    • 0028092853 scopus 로고
    • Congenital contractural arachnodactyly (Beals syndrome)
    • Viljoen D: Congenital contractural arachnodactyly (Beals syndrome). J Med Genet 1994; 31:640-643
    • (1994) J Med Genet , vol.31 , pp. 640-643
    • Viljoen, D.1
  • 7
    • 0023470783 scopus 로고
    • X-linked mental retardation with marfanoid habitus
    • Fryns JP, Buttiens M: X-linked mental retardation with marfanoid habitus. Am J Med Genet 1987; 28:267-274
    • (1987) Am J Med Genet , vol.28 , pp. 267-274
    • Fryns, J.P.1    Buttiens, M.2
  • 8
    • 0021357699 scopus 로고
    • A form of X-linked mental retardation with marfanoid habitus
    • Lujan JE, Carlis ME, Lubs HA: A form of X-linked mental retardation with marfanoid habitus. Am J Med Genet 1984; 17:311-322
    • (1984) Am J Med Genet , vol.17 , pp. 311-322
    • Lujan, J.E.1    Carlis, M.E.2    Lubs, H.A.3
  • 9
    • 0020308502 scopus 로고
    • The spectrum of cardiovascular disease in Marfan's syndrome: A clinico-morphologic study of 18 necropsy patients and comparison to 151 previously reported necropsy patients
    • Roberts WC, Hoing HS: The spectrum of cardiovascular disease in Marfan's syndrome: a clinico-morphologic study of 18 necropsy patients and comparison to 151 previously reported necropsy patients. Am Heart J 1982; 104:115-135
    • (1982) Am Heart J , vol.104 , pp. 115-135
    • Roberts, W.C.1    Hoing, H.S.2
  • 10
    • 0029031005 scopus 로고
    • Distinct skeletal abnormalities in four girls with Shprintzen-Goldberg syndrome
    • Ades LC, Morris LL, Power RG, et al: Distinct skeletal abnormalities in four girls with Shprintzen-Goldberg syndrome. Am J Med Genet 1995; 57:565-572
    • (1995) Am J Med Genet , vol.57 , pp. 565-572
    • Ades, L.C.1    Morris, L.L.2    Power, R.G.3
  • 11
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    • Ectopia lentis and aortic root dilatation in congenital contractual arachnodactyly
    • Bawle E, Quigg MH: Ectopia lentis and aortic root dilatation in congenital contractual arachnodactyly. Am J Med Genet 1992; 42:19-21
    • (1992) Am J Med Genet , vol.42 , pp. 19-21
    • Bawle, E.1    Quigg, M.H.2
  • 12
    • 0026510275 scopus 로고
    • Genetic linkage of the Marfan syndrome, ectopic lentis, and congenital contractual arachnodactyly to the fibrillin genes on chromosomes 15 and 5
    • Tsipouras P, Del Mastro R, Sarfarazi M, et al: Genetic linkage of the Marfan syndrome, ectopic lentis, and congenital contractual arachnodactyly to the fibrillin genes on chromosomes 15 and 5. N Engl J Med 1992; 326:905-909
    • (1992) N Engl J Med , vol.326 , pp. 905-909
    • Tsipouras, P.1    Del Mastro, R.2    Sarfarazi, M.3


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.