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Published on: August 15, 2019
A novel TAB2 mutation detected in a putative case of frontometaphyseal dysplasia
Asuka Hori1,2,3, Ohsuke Migita3,4, Rika Kawaguchi-Kawata1,2
1Department of Medical Genetics and Genomics, the Kitasato University Graduate School of Medical Sciences, Kanagawa, Japan.
Abstract:
Frontometaphyseal dysplasia (FMD) type 2 is an autosomal dominant disorder characterized by skeletal abnormalities and caused by MAP3K7 mutation. We identified a novel missense mutation in TAB2 associated with FMD in a child with multiple congenital malformations. This case was diagnosed as FMD due to joint contractures and bone deformities. This is the third report of FMD caused by a TAB2 mutation located in the TAK1-binding region.
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