1.
Clin Genet
; 28(3): 251-4, 1985 Sep.
Article
in English
| MEDLINE
| ID: mdl-4064363
ABSTRACT
A 14-month-old female infant with a syndrome mainly consisting of cortical blindness, psychomotor retardation and postaxial polydactyly (type B in hands and type A in feet) was studied. Two deceased sibs were similarly affected. Differential diagnosis and the review of medical literature permit the individualization of a distinct syndrome with a probable autosomal recessive pattern of inheritance.