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Genetic analysis of a child with mental retardation and hypospadia / 中华医学遗传学杂志
Article en Zh | WPRIM | ID: wpr-781317
Biblioteca responsable: WPRO
ABSTRACT
OBJECTIVE@#To carry out genetic testing for a boy presenting with mental retardation and hypoplasia.@*METHODS@#Conventional karyotyping, fluorescence in situ hybridization (FISH) and single nucleotide polymorphism based array (SNP-array) were used to analyze the boy and his parents.@*RESULTS@#SNP-array has detected a 25.7 Mb microduplication at 2q33.3q36.3 in the boy. Chromosomal karyotyping and FISH analysis indicated that his mother had a karyotype of 46,XX,ish ins(11;2) (p15;q33q36), and that the boy has carried an abnormal chromosome 11 derived from the maternal translocation. The karyotype of the boy was ascertained as 46,XY,ish der(11)ins(11;2) (p15;q33q36)mat.@*CONCLUSION@#SNP-array combined with G-banding and FISH can delineate the cryptic translocation and is valuable for the assessment of recurrence risk for subsequent pregnancies.
Asunto(s)
Texto completo: 1 Índice: WPRIM Asunto principal: Translocación Genética / Pruebas Genéticas / Bandeo Cromosómico / Hibridación Fluorescente in Situ / Polimorfismo de Nucleótido Simple / Duplicación Cromosómica / Genética / Hipospadias / Cariotipificación / Discapacidad Intelectual Tipo de estudio: Prognostic_studies Límite: Child / Female / Humans / Male / Pregnancy Idioma: Zh Revista: Chinese Journal of Medical Genetics Año: 2019 Tipo del documento: Article
Texto completo: 1 Índice: WPRIM Asunto principal: Translocación Genética / Pruebas Genéticas / Bandeo Cromosómico / Hibridación Fluorescente in Situ / Polimorfismo de Nucleótido Simple / Duplicación Cromosómica / Genética / Hipospadias / Cariotipificación / Discapacidad Intelectual Tipo de estudio: Prognostic_studies Límite: Child / Female / Humans / Male / Pregnancy Idioma: Zh Revista: Chinese Journal of Medical Genetics Año: 2019 Tipo del documento: Article