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Admas-Oliver syndrome is a rare autosomal dominant disease of congenital development defects association with aplasia cutis. All of 81 reported cases were of 32 group families. These two cases had congenital scalp cutis aplasia with developmental defect and hypoplasia of left foot digits in case 1.Congenital deaf-mute in both can added to the past known findings in this syndrome. Thoracic defor...
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ژورنال
عنوان ژورنال: Psychiatric Bulletin
سال: 2001
ISSN: 0955-6036,1472-1473
DOI: 10.1192/pb.25.2.77-a