Article
Craniofrontonasal syndrome: study of 41 patients.
American journal of medical genetics - 11 Jan 1996
Saavedra D, Richieri-Costa A, Guion-Almeida M L, Cohen M M
Abstract excerpt
Of 41 patients with craniofrontonasal syndrome, 35 were female and 6 were male. Although most cases were sporadic, 7 familial instances were found. Craniofrontonasal syndrome represents a unique, incompletely understood X-linked disorder. Unusual manifestations in females included thick, wiry, and curly hair (49%), anterior cranium bifidum (6%), axillary pterygia (9%), unilateral breast hypoplasia (postpubertal;...
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