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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...
Bewaard in:
| Hoofdauteurs: | , , , , , |
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| Formaat: | Artigo |
| Taal: | Inglês |
| Gepubliceerd in: |
Hospital das Clínicas da Faculdade de Medicina da Universidade de São Paulo
2010
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| Onderwerpen: | |
| Online toegang: | https://ncbi.nlm.nih.gov/pmc/articles/PMC2954737/ https://ncbi.nlm.nih.gov/pubmed/21049214 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1590/S1807-59322010000900009 |
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