Clinical and Biochemical Studies on Hereditary Erythrocyte Pyruvate Kinase Deficiency Associated with Chronic Hemolytic Anemia
山口医学 Volume 29 Issue 4
Page 307-320
published_at 1980-12
Title
慢性溶血性貧血を伴う遺伝性赤血球ピルビン酸キナーゼ異常性の臨床的生化学的研究
Clinical and Biochemical Studies on Hereditary Erythrocyte Pyruvate Kinase Deficiency Associated with Chronic Hemolytic Anemia
Creators
Ishida Yoji
Source Identifiers
Clinical and biochemical studies on herediatary erythrocyte pyruvate kinase deficiency (20 homozygotes) associated with chronic hemolytic anemia were performed. Analyses of abnormal PKs were performed according to the International Committee for Standardization in Haematoloy (ICSH) recommended (7 cases) whole parents were consanguineous and the other group consists of double heterozygotes (13 cases) whole parents were not consanguineous. There is no difference as to the onset age, clinical symptoms, the level of anemia and half-life of erythrocytes between true homozygous group and double heterozygous group…
Languages
jpn
Resource Type
journal article
Publishers
山口大学医学会
Date Issued
1980-12
File Version
Not Applicable (or Unknown)
Access Rights
metadata only access
Relations
[ISSN]0513-1731
[NCID]AN00243156
Schools
医学部