메뉴 건너뛰기




Volumn 52, Issue 4, 1997, Pages 231-234

Scalp defect, absence of nipples, ear anomalies, renal hypoplasia: Another case of Finlay-Marks syndrome

Author keywords

Autosomal dominant inheritance; Hypoplastic ears; Nipples hypoplasia; Renal insufficiency; Scalp defect

Indexed keywords

ADULT; ARTICLE; ATHELIA; AUTOSOMAL DOMINANT DISORDER; CASE REPORT; CATARACT; EAR MALFORMATION; FEMALE; HUMAN; KIDNEY FAILURE; KIDNEY HYPOPLASIA; PRIORITY JOURNAL; SCALP; SKIN DISEASE;

EID: 0030728694     PISSN: 00099163     EISSN: None     Source Type: Journal    
DOI: 10.1111/j.1399-0004.1997.tb02553.x     Document Type: Article
Times cited : (16)

References (21)
  • 1
    • 1842319975 scopus 로고
    • The Finlay-Marks (SEN) syndrome: Report of a new case and review of the literature
    • Aase JM, Wilroy SR. The Finlay-Marks (SEN) syndrome: report of a new case and review of the literature. Proc Greenwood Genet Center 1988: 7: 177-178.
    • (1988) Proc Greenwood Genet Center , vol.7 , pp. 177-178
    • Aase, J.M.1    Wilroy, S.R.2
  • 2
    • 0018637974 scopus 로고
    • Autosomal dominantly inherited cutis aplasia congenita, ear malformations, right-sided facial paresis, and dermal sinuses
    • Anderson CE, Hollister D, Szalay GC. Autosomal dominantly inherited cutis aplasia congenita, ear malformations, right-sided facial paresis, and dermal sinuses. Birth Defects Original Article Series XV(5B) 1979: 265-270.
    • (1979) Birth Defects Original Article Series XV(5B) , pp. 265-270
    • Anderson, C.E.1    Hollister, D.2    Szalay, G.C.3
  • 3
    • 0028351787 scopus 로고
    • Scalp-ear-nipple syndrome: Additional manifestations
    • Edwards MJ, McDonald D, Moore P, Rae J. Scalp-ear-nipple syndrome: additional manifestations. Am J Med Genet 1994: 50: 247-250.
    • (1994) Am J Med Genet , vol.50 , pp. 247-250
    • Edwards, M.J.1    McDonald, D.2    Moore, P.3    Rae, J.4
  • 4
    • 0029040780 scopus 로고
    • Aplasia cutis congenita and associated disorders: An update
    • Evers MEJ, Steijlen PM, Hamel BCJ. Aplasia cutis congenita and associated disorders: an update. Clin Genet 1995: 47: 295-301.
    • (1995) Clin Genet , vol.47 , pp. 295-301
    • Evers, M.E.J.1    Steijlen, P.M.2    Hamel, B.C.J.3
  • 5
    • 0018186685 scopus 로고
    • An hereditary syndrome of lumpy scalp, odd ears and rudimentary nipples
    • Finlay AY, Marks R. An hereditary syndrome of lumpy scalp, odd ears and rudimentary nipples. Br J Dermatol 1978: 99: 423-430.
    • (1978) Br J Dermatol , vol.99 , pp. 423-430
    • Finlay, A.Y.1    Marks, R.2
  • 6
    • 1842272920 scopus 로고
    • Familial congenital defect of the scalp
    • Frank L, Ruby A. Familial congenital defect of the scalp. Arch Dermatol 1957: 75: 266.
    • (1957) Arch Dermatol , vol.75 , pp. 266
    • Frank, L.1    Ruby, A.2
  • 7
    • 0023174768 scopus 로고
    • Congenital scalp defects with distal limb reduction anomalies
    • Fryns JP. Congenital scalp defects with distal limb reduction anomalies. J Med Genet 1987: 24: 493-496.
    • (1987) J Med Genet , vol.24 , pp. 493-496
    • Fryns, J.P.1
  • 9
    • 0025772077 scopus 로고
    • Aplasia cutis congenita associated with syndactyly and supernumerary nipples: Report of a second family with similar clinical findings
    • Halper S, Rubenstein D. Aplasia cutis congenita associated with syndactyly and supernumerary nipples: report of a second family with similar clinical findings. Pediatr Dermatol 1991: 8: 32-34.
    • (1991) Pediatr Dermatol , vol.8 , pp. 32-34
    • Halper, S.1    Rubenstein, D.2
  • 12
    • 0026646844 scopus 로고
    • Aplasia cutis congenita, cleft palate, epidermolysis bullosa, and ectrodactyly: A new syndrome?
    • Jones EM, Hersh JH, Yusk JW. Aplasia cutis congenita, cleft palate, epidermolysis bullosa, and ectrodactyly: a new syndrome? Pediatr Dermatol 1992: 9: 293-297.
    • (1992) Pediatr Dermatol , vol.9 , pp. 293-297
    • Jones, E.M.1    Hersh, J.H.2    Yusk, J.W.3
  • 13
    • 0014237645 scopus 로고
    • Complete breast absence in siblings
    • Kowlessar M, Orti E. Complete breast absence in siblings. Am J Dis Child 1968: 115: 91-92.
    • (1968) Am J Dis Child , vol.115 , pp. 91-92
    • Kowlessar, M.1    Orti, E.2
  • 14
    • 0023732558 scopus 로고
    • Congenital scalp defect with limb anomalies (Adams-Oliver syndrome): Report of ten cases and review of the literature
    • Kuster W, Lenz W, Kaariainen H, Majewski F. Congenital scalp defect with limb anomalies (Adams-Oliver syndrome): report of ten cases and review of the literature. Am J Med Genet 1988: 31: 99-115.
    • (1988) Am J Med Genet , vol.31 , pp. 99-115
    • Kuster, W.1    Lenz, W.2    Kaariainen, H.3    Majewski, F.4
  • 15
    • 0026309726 scopus 로고
    • Scalp defect, nipples absence and ears abnormalities: Another case of Finlay syndrome
    • Le Merrer M, Renier D, Briard ML. Scalp defect, nipples absence and ears abnormalities: another case of Finlay syndrome. Genet Couns 1991: 4: 233-236.
    • (1991) Genet Couns , vol.4 , pp. 233-236
    • Le Merrer, M.1    Renier, D.2    Briard, M.L.3
  • 16
    • 0022002390 scopus 로고
    • Odonto-onycho-dysplasia with alopecia: A new pure ectodermal dysplasia with probable autosomal recessive inheritance
    • Pinheiro M. Odonto-onycho-dysplasia with alopecia: a new pure ectodermal dysplasia with probable autosomal recessive inheritance. Am J Med Genet 1985: 20: 197-202.
    • (1985) Am J Med Genet , vol.20 , pp. 197-202
    • Pinheiro, M.1
  • 18
    • 0023856210 scopus 로고
    • Scalp and limb defects with cutis marmorata telangiectatica congenita: Adams-Oliver syndrome?
    • Toriello HV, Graff RG, Florentine MF, Lacina S, Moore WD. Scalp and limb defects with cutis marmorata telangiectatica congenita: Adams-Oliver syndrome? Am J Med Genet 1988: 29: 269-276.
    • (1988) Am J Med Genet , vol.29 , pp. 269-276
    • Toriello, H.V.1    Graff, R.G.2    Florentine, M.F.3    Lacina, S.4    Moore, W.D.5
  • 19
    • 0020679788 scopus 로고
    • New, autosomal dominant form of ectodermal dysplasia
    • Tuffli GA, Laxova R. New, autosomal dominant form of ectodermal dysplasia. Am J Med Genet 1983: 14: 381-384.
    • (1983) Am J Med Genet , vol.14 , pp. 381-384
    • Tuffli, G.A.1    Laxova, R.2
  • 20
    • 0015474523 scopus 로고
    • Dominant inheritance of absence of the breast
    • Wilson MG, Hall EB, Ebbin AJ. Dominant inheritance of absence of the breast. Humangenetik 1972: 14: 268-270.
    • (1972) Humangenetik , vol.14 , pp. 268-270
    • Wilson, M.G.1    Hall, E.B.2    Ebbin, A.J.3


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.