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Three new cases of Tel Hashomer camptodactyly syndrome in one Arabic family

✍ Scribed by Tylki-Szymanska, Anna ;Opitz, John M. ;Reynolds, James F.


Publisher
John Wiley and Sons
Year
1986
Tongue
English
Weight
227 KB
Volume
23
Category
Article
ISSN
0148-7299

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The Tel Hashomer camptodactyly syndrome:
✍ Pagnan, Nina Amalia Brancia ;Gollop, Thomaz Rafael ;Lederman, Henrique ;Optiz, J πŸ“‚ Article πŸ“… 1988 πŸ› John Wiley and Sons 🌐 English βš– 347 KB πŸ‘ 3 views

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.