Description of the disease * EnglishPolish Pobierz sekcję do PDF Definicja A rare genetic multiple congenital anomalies/dysmorphic syndrome characterized by aplasia cutis congenita of the scalp, breast anomalies ranging from hypothelia or athelia to amastia, and anomalies of the external ears. Variable clinical characteristics include nail and dental anomalies, syndactyly and camptodactyly of fingers and/or toes, sparse or absent secondary sexual hair, renal malformations, and facial dysmorphism. Cases with severe hypotonia and developmental delay have been reported. Disease data Klasyfikacja Malformation syndrome Synonimy Finlay-Marks syndrome Zespół Finlay'a i Marksa Kod ORPHA 2036 Kod OMIM 181270 Kod ICD10 Q87.8 Kod ICD11 LD27.0Y *Soruce Extended description of the disease Pobierz sekcję do PDF No additional description. Orphanet - interntowa baza danych dotyczących rzadkich chorób i sierochych leków. ©INSERM 1999 - Dostępna na stronie www.orphanet.pl