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Updated: Jul 19, 2026

Investigating the Pathogenesis of MYH7 Mutation Gly823Glu in Familial Hypertrophic Cardiomyopathy using a Mouse Model
Published on: August 8, 2022
Nager's acrofacial dysostosis with hypertrophic cardiomyopathy
Mahdi Kahrom1, Mohammad R Abbaszadegan, Hadi Kahrom
1Division of Human Genetics, Immunology Research Center, Bu-Ali Research Institute, Mashhad, Iran.
Abstract:
Nager syndrome is a rare condition associated with craniofacial malformations such as, micrognathia, zygomatic hypoplasia, external ear malformations, and preaxial limb deformities. This report features a case of Nager syndrome occurring in a one-year-old boy showing microretrognathia, thumb hypoplasia, brachydactyly, hexadactyly, and hypertrophic cardiomyopathy, characteristics not usually encountered in published cases.
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