Scalp-ear-nipple syndrome

Orpha code: 2036OMIM code: 181270

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

No additional description.

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