Article
mRNA analysis revealed a novel pathogenic EIF2S3 variant causing MEHMO syndrome.
European journal of medical genetics - 1 Feb 2022
Ivanova Nadezda, Serzhanova Victoria, Demina Nina, Guseva Darya, Skoblov Mikhail
Abstract excerpt
EIF2S3 pathogenic variants have been shown to cause MEHMO syndrome - a rare X-linked intellectual disability syndrome. In most cases, DNA diagnostics of MEHMO syndrome is performed using exome sequencing. We describe two cousins with profound intellectual disability, severe microcephaly, microgenitalism, hypoglycemia, epileptic seizures, and hypertrichosis, whose clinical symptoms allowed us to suspect MEHMO...
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