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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...
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| Publicado no: | Korean J Pediatr |
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| Main Authors: | , , , , , |
| Formato: | Artigo |
| Idioma: | Inglês |
| Publicado em: |
The Korean Pediatric Society
2015
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| Assuntos: | |
| Acesso em linha: | https://ncbi.nlm.nih.gov/pmc/articles/PMC4388972/ https://ncbi.nlm.nih.gov/pubmed/25861334 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.3345/kjp.2015.58.3.108 |
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