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Das Bhowmik, A. and Vijayalakshmi, S.R. and Dalal, Ashwin (2018) Tarsal-carpal coalition syndrome: Report of a novel missense mutation in NOG gene and phenotypic delineation. American Journal of Medical Genetics Part A, 176 (1). pp. 219-224. ISSN 1552-4825

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Abstract

We report a family of Indian origin presenting with Tarsal-carpal coalition syndrome (TCC), which is a rare genetic disorder of skeletal abnormalities, inherited in autosomal dominant manner. In this family, three individuals (mother and two children) were found to be similarly affected with slight intrafamilial individual variability in the phenotype. Sanger sequencing revealed a novel heterozygous missense mutation in NOG gene (NM_005450.4:c.611G>A) in all the affected individuals of the family. Until now only six mutations have been reported in different families affected with TCC syndrome worldwide. This report further delineates the phenotypic spectrum of this rare disorder with the addition of a new variant to the mutation spectrum.

Item Type: Article
Depositing User: Dr P Divakar
Date Deposited: 24 Nov 2017 11:53
Last Modified: 26 Apr 2018 19:26
URI: http://cdfd.sciencecentral.in/id/eprint/811

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