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Review
. 1997 Oct;52(4):231-4.
doi: 10.1111/j.1399-0004.1997.tb02553.x.

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

G Plessis  1 , M Le Treust, M Le Merrer
Affiliations
Review

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

G Plessis et al. Clin Genet. 1997 Oct.

Abstract

The association of scalp defect, unusual ears and absence of nipples was described by Finlay & Marks as an autosomal dominant trait. We report a new case in a 23-year-old woman. Renal insufficiency and cataract seem to be frequent and must be investigated.

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