Literature DB >> 1153954

A new variant of erythrocyte pyruvate kinase - PK "maebashi".

K Kubota, M Moteki, M Omine, J Tsuchya, T Maekawa, S Miwa.   

Abstract

A new case of erythrocyte pyruvate kinase deficiency was described. - A 9 year-old male patient was hospitalized because of anaemia, jaundice and splenomegaly. Diagnosis was made primarily on the basis of the erythrocyte enzyme studies. Because the pyruvate kinase of this patient demonstrated certain different characteristics from the other variants described previously, it was tentatively designated PK "Maebashi".

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Year:  1975        PMID: 1153954     DOI: 10.1111/j.1600-0609.1975.tb02423.x

Source DB:  PubMed          Journal:  Scand J Haematol        ISSN: 0036-553X


  1 in total

1.  Hereditary erythrocyte pyruvate-kinase (PK) deficiency and chronic hemolytic anemia: clinical, genetic and molecular studies in six new Spanish patients.

Authors:  J L Vives-Corrons; J Marie; M A Pujades; A Kahn
Journal:  Hum Genet       Date:  1980       Impact factor: 4.132

  1 in total

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