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Genetic analysis and prenatal diagnosis of a fetus with Xq25 microduplication / 中华医学遗传学杂志
Chinese Journal of Medical Genetics ; (6): 425-427, 2022.
Artigo em Chinês | WPRIM | ID: wpr-928434
ABSTRACT
OBJECTIVE@#To explore the genetic basis for a fetus with structural brain abnormalities.@*METHODS@#The karyotypes of the fetus and its parents were analyzed by conventional G-banding. Chromosome microarray analysis (CMA) was carried out to detect chromosomal microdeletion and microduplication.@*RESULTS@#No kartotypic abnormality was detected in the fetus and its parents. CMA has identified a 194 kb microduplication at Xq25 in the fetus, which encompassed exons 4-35 of the STAG2 gene and was derived from its mother.@*CONCLUSION@#The Xq25 duplication encompassing part of the STAG2 gene probably underlay the brain malformation in the fetus.
Assuntos
Texto completo: DisponíveL Índice: WPRIM (Pacífico Ocidental) Assunto principal: Diagnóstico Pré-Natal / Testes Genéticos / Bandeamento Cromossômico / Feto / Cariotipagem Tipo de estudo: Estudo diagnóstico Limite: Feminino / Humanos / Gravidez Idioma: Chinês Revista: Chinese Journal of Medical Genetics Ano de publicação: 2022 Tipo de documento: Artigo

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Texto completo: DisponíveL Índice: WPRIM (Pacífico Ocidental) Assunto principal: Diagnóstico Pré-Natal / Testes Genéticos / Bandeamento Cromossômico / Feto / Cariotipagem Tipo de estudo: Estudo diagnóstico Limite: Feminino / Humanos / Gravidez Idioma: Chinês Revista: Chinese Journal of Medical Genetics Ano de publicação: 2022 Tipo de documento: Artigo