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Updated: Jun 27, 2025

Investigating the Pathogenesis of MYH7 Mutation Gly823Glu in Familial Hypertrophic Cardiomyopathy using a Mouse Model
Published on: August 8, 2022
Hypertension and Brachydactyly Syndrome: Genetic Insights and a Novel Presentation
Abdulla Shahid1, Naman S Shetty1, Nirav Patel1
1Division of Cardiovascular Disease, University of Alabama at Birmingham, Birmingham, Alabama, USA.
Abstract:
Phosphodiesterase 3A (PDE3A) gene mutations have recently been associated with hypertension and brachydactyly syndrome (HTNB). This report shows how the recent recognition of the role of the PDE3A gene in HTNB facilitated the diagnosis of HTNB in a 20-year-old female who could not be diagnosed at her initial presentation at 6 years of age.
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