Scalp-ear-nipple (Finlay-Marks) syndrome: A familial case with renal involvement [4]

Clinical Genetics

Volumn 56, Issue 2, 1999, Pages 170-172

  Picard, C ^a   Couderc, S ^a   Skojaei, T ^a   Salomon, R ^a   De Lonlay, P ^a   Le Merrer, M ^a   Munnich, A ^a   Lyonnet, S ^a   Amiel, J ^a  

^a HÔPITAL NECKER ENFANTS MALADES   (France)

Author keywords

[No Author keywords available]

Indexed keywords

ADULT; CASE REPORT; CONGENITAL MALFORMATION; EAR MALFORMATION; FACE DYSMORPHIA; FEMALE; FINLAY MARKS SYNDROME; HAIR LOSS; HUMAN; INFANT; KIDNEY DISEASE; LETTER; MALE; NEWBORN; NIPPLE; PRIORITY JOURNAL; PYELONEPHRITIS; SCALP; URINARY TRACT MALFORMATION;

EID: 0032875317     PISSN: 00099163     EISSN: None     Source Type: Journal    
DOI: 10.1034/j.1399-0004.1999.560216.x     Document Type: Letter

References (6)

1. 1 Aase JM & Wilroy SR. The Finlay–Marks (SEN) syndrome: report of a new case and review of literature. Proc Greenwood Genet Center 1988: 7: 177 178.
2. 2 Edwards MJ, McDonald D, Moore P, Rae J. Scalp‐Ear‐Nipple syndrome: additional manifestations. Am J Med Genet 1994: 50: 247 250.
3. 3 Finlay AY & Marks R. An hereditary syndrome of lumpy scalp, odd ears and rudimentary nipples. Brit J Dermatol 1978: 99: 423 430.
4. 4 Le Merrer M, Renier D, Briard ML. Scalp defect, nipples absence and ear abnormalities: an other case of Finlay syndrome. Genet Couns 1991: 4: 233 236.
5. 5 Plessis G, Le Treust M, Le Merrer M. Scalp defect, nipples, ear anomalies, renal hypoplasia: another case of Finlay–Marks syndrome. Clin Genet 1997: 52: 231 234.
6. 6 Tuffli GA & Laxova R. New, autosomal dominant form of ectodermal dysplasia. Am J Med Genet 1983: 14: 381 383.