Literature DB >> 1497965

Homozygous pyruvate kinase deficiency in Hong Kong ethnic minorities.

D C Wei1, L C Chan, A Li.   

Abstract

Three cases of pyruvate kinase (PK) deficiency resulting in congenital haemolytic anaemia with transfusion dependency are described. These cases resulted from consanguineous marriages in non-Han Chinese and include a pair of twins. We believe this to be the first documentation of homozygous PK deficiency in the Hong Kong population. The diagnosis was masked due to transfusion dependency in each case stressing the need to take a sample of pretransfusion blood for PK enzyme assay, and for family studies, when this disorder is suspected.

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Year:  1992        PMID: 1497965     DOI: 10.1111/j.1440-1754.1992.tb02682.x

Source DB:  PubMed          Journal:  J Paediatr Child Health        ISSN: 1034-4810            Impact factor:   1.954


  1 in total

1.  Case reports of metabolic disorders from Nepal.

Authors:  Arti Sharma Pandey
Journal:  Mol Genet Metab Rep       Date:  2019-11-19
  1 in total

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