A Case of Turner Syndrome with Concomitant Transient Hypogammaglobulinaemia of Infancy and Central Diabetes Insipidus

Turner syndrome (TS) is a genetic disorder that affects development in females and is characterized by the complete or partial absence of the second sex chromosome, or monosomy X. TS is associated with abnormalities in lymphatic and skeletal development, in growth, and in gonadal function. Cardiac a...

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Detalles Bibliográficos
Autores principales: Korkmaz, Hüseyin Anıl, Özkan, Behzat, Hazan, Filiz, Büyükinan, Muammer, Çelik, Tanju
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Galenos Publishing 2013
Materias:
Case Report
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3628396/
https://www.ncbi.nlm.nih.gov/pubmed/23419422
http://dx.doi.org/10.4274/Jcrpe.880

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3628396/
https://www.ncbi.nlm.nih.gov/pubmed/23419422
http://dx.doi.org/10.4274/Jcrpe.880

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