Identification of X Monosomy Cells From a Gonad of Mixed Gonadal Dysgenesis With a 46,XY Karyotype: Case Report

Mixed gonadal dysgenesis (MGD) is a disorder of sexual development that typically has a mosaic 45,X/46,XY karyotype. A 1-year-old infant with 46,XY identified by peripheral blood karyotype demonstrated clinical manifestations and gonadal pathologic features of MGD. Fluorescence in situ hybridization...

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Detalles Bibliográficos
Autores principales: Nishina-Uchida, Noriko, Fukuzawa, Ryuji, Hasegawa, Yukihiro, Morison, Ian M.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Wolters Kluwer Health 2015
Materias:
3500
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4554039/
https://www.ncbi.nlm.nih.gov/pubmed/25860218
http://dx.doi.org/10.1097/MD.0000000000000720

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4554039/
https://www.ncbi.nlm.nih.gov/pubmed/25860218
http://dx.doi.org/10.1097/MD.0000000000000720

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