A Japanese neonatal case of glucose-6-phosphate dehydrogenase deficiency presenting as severe jaundice and hemolytic anemia without apparent trigger

BACKGROUND: Glucose-6-phosphate dehydrogenase (G6PD) deficiency is rare among Japanese ethnicity although it is known as one of the most common hereditary disorders of erythrocytes, causing intravascular hemolysis. It is well-known that G6PD deficiency may cause hemolysis even in the neonatal period...

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Hlavní autoři: Tsuzuki, Shinya, Akahira-Azuma, Moe, Kaneshige, Masao, Shoya, Kazuhiro, Hosokawa, Shinichi, Kanno, Hitoshi, Matsushita, Takeji
Médium: Artigo
Jazyk:Inglês
Vydáno: Springer International Publishing 2013
Témata:
Short Report
On-line přístup:https://ncbi.nlm.nih.gov/pmc/articles/PMC3776087/
https://ncbi.nlm.nih.gov/pubmed/24052930
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1186/2193-1801-2-434
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