A Japanese neonatal case of glucose-6-phosphate dehydrogenase deficiency presenting as severe jaundice and hemolytic anemia without apparent trigger-Reference-Cited by-同舟云学术

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

Published:2013-09-04 Issue:1 Volume:2 Page:
ISSN:2193-1801
Container-title:SpringerPlus
language:en
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Author:

Tsuzuki Shinya,Akahira-Azuma Moe,Kaneshige Masao,Shoya Kazuhiro,Hosokawa Shinichi,Kanno Hitoshi,Matsushita Takeji

Publisher

Springer Science and Business Media LLC

Subject

Multidisciplinary

Link

http://link.springer.com/content/pdf/10.1186/2193-1801-2-434.pdf

Reference14 articles.

1. Akazawa Y, et al.: A case of glucose-6-phosphate dehydrogenase deficiency with acute hemolytic anemia. J Japan Soc Premature Newborn Med 2011, 23: 108-123.

2. Beutler E: G6PD deficiency. Blood 1994, 84: 3613-3636.

3. Cappellini MD, Fiorelli G: Glucose-6-phosphate dehydrogenase deficiency. Lancet 2008, 371: 64-74. 10.1016/S0140-6736(08)60073-2

4. Department of Pediatrics, Kobe University Graduate School of Medicine: The management of preterm neonates. Tokyo: Nihon Shoni Iji Syuppansya; 1993:205-224.

5. Dhillon AS, et al.: Massive acute haemolysis in neonates with glucose-6-phosphate dehydrogenase deficiency. Arch Dis Child Fetal Neonatal Ed 2003, 88: F534-F536. 10.1136/fn.88.6.F534

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