Clinical variability of chromosome 22q11.2 deletion syndrome

22q11.2 deletion syndrome (22q11.2 DS) is a disorder that has multiple symptoms and affects various organs and systems. Despite the great variability of clinical manifestations, common 22q11.2 DS includes congenital heart defect, immunodeficiency, characteristic facial features, palatal defects, dev...

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Detalles Bibliográficos
Autores principales: Boyarchuk, Oksana, Volyanska, Liubov, Dmytrash, Liubov
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Polish Society of Experimental and Clinical Immunology 2017
Materias:
Case Report
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5820982/
https://www.ncbi.nlm.nih.gov/pubmed/29472823
http://dx.doi.org/10.5114/ceji.2017.72818

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5820982/
https://www.ncbi.nlm.nih.gov/pubmed/29472823
http://dx.doi.org/10.5114/ceji.2017.72818

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