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De novo start-loss variant in HIRA in patient with DiGeorge-like syndrome
Dmitry Maslennikov1, Ekaterina Tolmacheva1, Jekaterina Shubina1
1National Medical Research Center for Obstetrics, Gynecology and Perinatology of the Ministry of Health of the Russian Federation, Moscow, Russia.
Abstract:
A case of a newborn with tetralogy of Fallot, corpus callosum hypoplasia, and phenotypic features similar to DiGeorge syndrome. Chromosomal microarray analysis did not reveal any alterations. Whole exome sequencing and Sanger sequencing identified a de novo variant in the HIRA gene resulting in the loss of the start codon.
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