Glucose-6-phosphate dehydrogenase deficiency--report of 4 cases

Glucose-6-phosphate dehydrogenase (G6PD) deficiency is the most common hereditary enzyme disorder and more than 200 million people have a deficiency in this enzyme. It is a globally important cause of neonatal jaundice and causes life-threatening hemolytic crisis in childhood. At later ages, certain...

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Veröffentlicht in:	Journal of Korean medical science 1992-03, Vol.7 (1), p.71-75
Hauptverfasser:	Kim, M K, Yang, C H, Kang, S H, Lyu, C J, Kim, K Y
Format:	Artikel
Sprache:	eng
Schlagworte:	Child Child, Preschool Glucosephosphate Dehydrogenase Deficiency - diagnosis Glucosephosphate Dehydrogenase Deficiency - genetics Humans Male Pedigree
Online-Zugang:	Volltext
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