Kernicterus by glucose-6-phosphate dehydrogenase deficiency: a case report and review of the literature

INTRODUCTION: Glucose-6-phosphate dehydrogenase deficiency is an X-linked recessive disease that causes acute or chronic hemolytic anemia and potentially leads to severe jaundice in response to oxidative agents. This deficiency is the most common human innate error of metabolism, affecting more than...

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Detalles Bibliográficos
Autores principales: de Gurrola, Gladys Cossio, Araúz, Juan José, Durán, Elfilda, Aguilar-Medina, Maribel, Ramos-Payán, Rosalío, García-Magallanes, Noemí, Pacheco, Gerardo Vaca, Meraz, Eliakym Arámbula
Formato: Texto
Lenguaje:English
Publicado: BioMed Central 2008
Materias:
Case Report
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2391151/
https://www.ncbi.nlm.nih.gov/pubmed/18460213
http://dx.doi.org/10.1186/1752-1947-2-146

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2391151/
https://www.ncbi.nlm.nih.gov/pubmed/18460213
http://dx.doi.org/10.1186/1752-1947-2-146

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