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• W2136985612 abstract "Due to the genetic and clinical heterogeneity of Rett syndrome, patients with nonclassic phenotypes are classified as an atypical Rett syndrome, that is, preserved speech variant, early seizure variant, and congenital variant. Respectively, MECP2, CDKL5, and FOXG1 have been found to be the causative genes, but FOXG1 variants are the rarest and least studied. We performed mutational analyses for FOXG1 on 11 unrelated patients without MECP2 and CDKL5 mutations, who were diagnosed with atypical Rett syndrome. One patient, who suffered from severe early-onset mental retardation and multiple-type intractable seizures, carried a novel, de novo FOXG1 mutation (p.Gln70Pro). This case concurs with previous studies that have reported yields of ∼10%. FOXG1-related atypical Rett syndrome is rare in Korean population, but screening of this gene in patients with severe mental retardation, microcephaly, and early-onset multiple seizure types without specific genetic causes can help broaden the phenotypic spectrum of the distinct FOXG1-related syndrome." @default.
• W2136985612 created "2016-06-24" @default.
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• W2136985612 date "2015-02-10" @default.
• W2136985612 modified "2023-10-11" @default.
• W2136985612 title "<i>FOXG1</i> Mutation is a Low-Incidence Genetic Cause in Atypical Rett Syndrome" @default.
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• W2136985612 doi "https://doi.org/10.1177/2329048x14568151" @default.
• W2136985612 hasPubMedCentralId "https://www.ncbi.nlm.nih.gov/pmc/articles/5417036" @default.
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