Biallelic HERC1 mutations in a syndromic form of overgrowth and intellectual disability
O Ortega-Recalde1, O I Beltrán2,3, J M Gálvez1
1Unidad de Genética, Grupo GENIUROS, Escuela de Medicina y Ciencias de la Salud, Universidad del Rosario, Bogotá, Colombia.
Clinical Genetics
|July 4, 2015
Abstract:
We report two Colombian siblings affected by overgrowth, intellectual disability and facial dysmorphism. Exome (via NGS) and Sanger sequencing revealed that biallelic sequence variants in a novel gene (HERC1) might be related to the disease pathogenesis. These results provide useful data for future genotype-phenotype correlations and for a molecular diagnosis of overgrowth.
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