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- W2896844138 abstract "Abstract The GATA zing finger domain‐containing protein 2B ( GATAD2B ) gene encodes the p66beta protein, a subunit of the MeCP1‐Mi2/ nucleosome remodeling and deacetylase complex, which is involved in transcription regulation and chromatin remodeling. Pathogenic variants in the GATAD2B gene have recently been associated with a recognizable neurodevelopmental syndrome, characterized by intellectual disability, limited speech, childhood hypotonia, and dysmorphic features. The majority of reported patients resulted from de novo loss of function (LOF) variants. We report a patient identified through whole exome sequencing analysis where a healthy mother was found to be low level mosaic for the pathogenic LOF variant found in her child, who is affected with GATAD2B ‐associated neurodevelopmental disorder (GAND). This variant was only found with the use of next generation sequencing technology in the mother and confirmed by digital droplet PCR. We summarize additional patients with GATAD2B LOF variants from a literature review and with our patient we contribute to delineate the phenotypic spectrum of GAND. We highlight the importance of detailed genetic testing, testing method, and counseling for cases of somatic mosaicism in an unaffected parent of children with GAND. This inheritance may be underreported and has a direct impact on reproductive planning and prenatal diagnosis." @default.
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- W2896844138 date "2018-10-22" @default.
- W2896844138 modified "2023-09-26" @default.
- W2896844138 title "Intellectual disability due to monoallelic variant in <i>GATAD2B</i> and mosaicism in unaffected parent" @default.
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- W2896844138 doi "https://doi.org/10.1002/ajmg.a.40667" @default.
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