Literature DB >> 3080188

Glucose-6-phosphate dehydrogenase deficiency: a preventable cause of mental retardation.

H Singh.   

Abstract

Over two years cord blood from 27 879 babies was screened for glucose-6-phosphate dehydrogenase (G6PD) deficiency. The overall incidence was 3.1% in boys and 1.6% in girls. Sixty nine babies had severe jaundice (bilirubin concentration greater than 380 mmol/l (20 mg/100 ml], and exchange transfusion was performed. Parents were given written and verbal instructions to avoid herbs and drugs that trigger kernicterus, which reduced the incidence of kernicterus and thereby prevented mental retardation. G6PD deficiency is common in all three ethnic groups (Malays, Chinese, and Indians) in Malaysia and screening is recommended.

Entities:  

Mesh:

Year:  1986        PMID: 3080188      PMCID: PMC1339365          DOI: 10.1136/bmj.292.6517.397

Source DB:  PubMed          Journal:  Br Med J (Clin Res Ed)        ISSN: 0267-0623


  3 in total

1.  Newborn screening in the Asia Pacific region.

Authors:  Carmencita D Padilla; Bradford L Therrell
Journal:  J Inherit Metab Dis       Date:  2007-07-23       Impact factor: 4.982

Review 2.  Glucose-6-Phosphate Dehydrogenase Deficiency and Neonatal Hyperbilirubinemia: Insights on Pathophysiology, Diagnosis, and Gene Variants in Disease Heterogeneity.

Authors:  Heng Yang Lee; Azlin Ithnin; Raja Zahratul Azma; Ainoon Othman; Armindo Salvador; Fook Choe Cheah
Journal:  Front Pediatr       Date:  2022-05-24       Impact factor: 3.569

3.  Use of reflective materials during phototherapy for newborn infants with unconjugated hyperbilirubinaemia.

Authors:  Hans Van Rostenberghe; Jacqueline J Ho; Choo Hau Lim; Intan Juliana Abd Hamid
Journal:  Cochrane Database Syst Rev       Date:  2020-07-01
  3 in total

北京卡尤迪生物科技股份有限公司 © 2022-2023.