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The Tel Hashomer camptodactyly syndrome: Report of a new case and review of the literature

✍ Scribed by Pagnan, Nina Amalia Brancia ;Gollop, Thomaz Rafael ;Lederman, Henrique ;Optiz, John M. ;Reynolds, James F.

Publisher
John Wiley and Sons
Year
1988
Tongue
English
Weight
347 KB
Volume
29
Category
Article
ISSN
0148-7299

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✦ Synopsis

We report on a new case of Tel Hashomer camptodactyly syndrome and review the literature. This syndrome is characterized by skeletal dysplasia, muscle hypoplasia, camptodactyly, and abnormal dermatoglyphics. The inheritance is autosomal recessive with probable partial expression in the heterozygote.

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