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Article in English | IMSEAR | ID: sea-89123

ABSTRACT

Two new cases with the Tel-Hashomer camptodactyly syndrome have been ascertained in an Indian family. This report emphasizes the autosomal recessive nature of disease and documents an additional feature of hirsuitism not previously described. The gene for Tel-Hashomer camptodactyly syndrome is present in all populations around the world.


Subject(s)
Abnormalities, Multiple/genetics , Adult , DNA-Binding Proteins/genetics , Female , Hand Deformities, Congenital/complications , Hirsutism/complications , Humans , Nuclear Proteins/genetics , Proto-Oncogene Proteins c-ets , Repressor Proteins/genetics , Siblings , Syndrome
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