G. Plessis et al., SCALP DEFECT, ABSENCE OF NIPPLES, EAR ANOMALIES, RENAL HYPOPLASIA - ANOTHER CASE OF FINLAY-MARKS-SYNDROME, Clinical genetics, 52(4), 1997, pp. 231-234
The association of scalp defect, unusual ears and absence of nipples w
as described by Finlay & Marks as an autosomal dominant trait. We repo
rt a new case in a 23-year-old woman. Renal insufficiency and cataract
seem to be frequent and must be investigated.