DiGeorge syndrome who developed lymphoproliferative mediastinal mass

DiGeorge syndrome is an immunodeficient disease associated with abnormal development of 3rd and 4th pharyngeal pouches. As a hemizygous deletion of chromosome 22q11.2 occurs, various clinical phenotypes are shown with a broad spectrum. Conotruncal cardiac anomalies, hypoplastic thymus, and hypocalce...

Descripción completa

Detalles Bibliográficos
Autores principales: Kim, Kyu Yeun, Hur, Ji Ae, Kim, Ki Hwan, Cha, Yoon Jin, Lee, Mi Jung, Kim, Dong Soo
Formato: Online Artículo Texto
Lenguaje:English
Publicado: The Korean Pediatric Society 2015
Materias:
Case Report
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4388972/
https://www.ncbi.nlm.nih.gov/pubmed/25861334
http://dx.doi.org/10.3345/kjp.2015.58.3.108

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4388972/
https://www.ncbi.nlm.nih.gov/pubmed/25861334
http://dx.doi.org/10.3345/kjp.2015.58.3.108

Ejemplares similares