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Pseudoisodicentric X chromosome in a female with primary amenorrhea
Journal of Genetic Medicine ; : 61-64, 2008.
Artigo em Coreano | WPRIM | ID: wpr-62799
ABSTRACT
A 24-year-old female with primary amenorrhea was referred for a chromosome study. The karyotype of the patient was 46,X,der(X) under initial GTG-banding analysis. Fluorescence in situ hybridization (FISH) analysis with an LSI Kallmann (KAL) region probe [probes for Xp22.3(KAL) and CEP(X) for control] was carried out. The abnormal chromosome was KAL- and CEP(X)x2. In addition, interphase FISH analysis revealed the patient to be mosaic for two different cell lines 90% of cells had three signals and 10% of the cells had only one signal for CEP(X). Based on these results, the karyotype of the patient was 45,X/46,X,psu idic(X)(p22.1), which is partial trisomy for Xqter-->Xp22.1 and partial monosomy for Xpter-->Xp22.1. This karyotype was considered a variant of Turner syndrome. In summary, Idic(X) and low-level mosaicism was successfully characterized by FISH analysis with a CEP(X) probe.
Assuntos

Texto completo: DisponíveL Índice: WPRIM (Pacífico Ocidental) Assunto principal: Trissomia / Síndrome de Turner / Cromossomo X / Deleção Cromossômica / Hibridização In Situ / Cariótipo / Fluorescência / Amenorreia / Interfase / Mosaicismo Limite: Feminino / Humanos Idioma: Coreano Revista: Journal of Genetic Medicine Ano de publicação: 2008 Tipo de documento: Artigo

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Texto completo: DisponíveL Índice: WPRIM (Pacífico Ocidental) Assunto principal: Trissomia / Síndrome de Turner / Cromossomo X / Deleção Cromossômica / Hibridização In Situ / Cariótipo / Fluorescência / Amenorreia / Interfase / Mosaicismo Limite: Feminino / Humanos Idioma: Coreano Revista: Journal of Genetic Medicine Ano de publicação: 2008 Tipo de documento: Artigo