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Tel Hashomer camptodactyly syndrome: 12-year follow-up of a Hungarian patient and review

✍ Scribed by Béla Melegh; Katalin Hollódy; Mária Aszmann; Károly Méhes


Publisher
John Wiley and Sons
Year
2005
Tongue
English
Weight
200 KB
Volume
135A
Category
Article
ISSN
1552-4825

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The Tel Hashomer camptodactyly syndrome:
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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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