DiGeorge Syndrome: a not so rare disease

INTRODUCTION: The DiGeorge Syndrome was first described in 1968 as a primary immunodeficiency resulting from the abnormal development of the third and fourth pharyngeal pouches during embryonic life. It is characterized by hypocalcemia due to hypoparathyroidism, heart defects, and thymic hypoplasia...

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Detalles Bibliográficos
Autores principales: Fomin, Angela BF, Pastorino, Antonio Carlos, Kim, Chong Ae, Pereira, Alexandre C, Carneiro‐Sampaio, Magda, Abe Jacob, Cristina Miuki
Formato: Texto
Lenguaje:English
Publicado: Hospital das Clínicas da Faculdade de Medicina da Universidade de São Paulo 2010
Materias:
Clinical Science
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2954737/
https://www.ncbi.nlm.nih.gov/pubmed/21049214
http://dx.doi.org/10.1590/S1807-59322010000900009

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2954737/
https://www.ncbi.nlm.nih.gov/pubmed/21049214
http://dx.doi.org/10.1590/S1807-59322010000900009

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