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  • Title: Scalp defect, absence of nipples, ear anomalies, renal hypoplasia: another case of Finlay-Marks syndrome.
    Author: Plessis G, Le Treust M, Le Merrer M.
    Journal: Clin Genet; 1997 Oct; 52(4):231-4. PubMed ID: 9383029.
    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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