| Literature DB >> 14226101 |
Abstract
Seven male newborns of Chinese, Greek and Italian origin presented with severe hemolytic jaundice due to red cell glucose-6-phosphate dehydrogenase (G-6-PD) deficiency. In five, the hemolysis was precipitated by inhalation of mothball vapours in the home. Kernicterus was evident upon admission in six infants and was fatal in four of these.G-6-PD deficiency should be suspected as a cause of jaundice in all full-term male infants of these ethnic groups. The diagnosis can be confirmed in any hospital by the methemoglobin reduction test. In areas similar to Toronto, Canada, where these high-risk ethnic groups prevail, the following measures are recommended: (1) detection of G-6-PD deficient newborns by screening cord bloods of all infants of these ethnic groups; (2) protection of affected infants from potentially hemolytic agents such as naphthalene, certain vitamin K preparations, and sulfonamides; and (3) observation of serum bilirubin levels to assess the need for exchange transfusion for hyperbilirubinemia.Entities:
Keywords: ANALGESICS AND ANTIPYRETICS; ANTIMALARIALS; BIOCHEMISTRY; CANADA; CAUCASIAN RACE; DRUG THERAPY; ETHNOLOGY; GENETICS, HUMAN; GLUCOSEPHOSPHATE DEHY- DROGENASE DEFICIENCY; INFANT, NEWBORN; INFANT, NEWBORN, DISEASES; JAUNDICE, NEONATAL; KERNICTERUS; METHEMOGLOBIN; MONGOLOID RACE; NADP; NAPHTHALENES; NITROFURANS; SEX; STATISTICS; SULFONAMIDES; TOXICOLOGIC REPORT
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Year: 1964 PMID: 14226101 PMCID: PMC1927448
Source DB: PubMed Journal: Can Med Assoc J ISSN: 0008-4409 Impact factor: 8.262