Guadalajara camptodactyly syndrome type I. A corroborative family
Abstract
Three sibs, two girls aged 18 and 9 years, and a 7‐year‐old boy, were found to have Guadalajara camptodactyly syndrome type I (GCSI). They had intrauterine growth retardation, dwarfism, peculiar facial appearance, camptodactyly and skeletal anomalies. Comparison with other camptodactyly syndromes led to the conclusion that the patients had the same disorder as the two first reported patients with GCSI. The clinical and radiological concordance...
Paper Details
Title
Guadalajara camptodactyly syndrome type I. A corroborative family
Published Date
Jan 1, 1993
Journal
Volume
43
Issue
1
Pages
11 - 15
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