1.
Clin Dysmorphol
; 16(2): 105-107, 2007 Apr.
Artigo
em Inglês
| MEDLINE
| ID: mdl-17351354
RESUMO
We report two children from an inbred Arab family with features suggestive of scalp-ear-nipple syndrome who in addition had severe hypotonia and developmental delay. Also addition, other features seen in scalp-ear-nipple syndrome such as camptodactyly, syndactyly and dry skin were absent in these children. We suggest the children in this report have a severe recessive form of this syndrome.