Hereditary haemolytic anaemia due to red cell pyrimidine 5‘‐nucleotidase deficiency in two Irish families with a note on the benefit of splenectomy

J. N. McMAHON, J. E. LIEBERMAN, E. C. GORDON‐SMITH, E. L. EGAN

Research output: Contribution to a Journal (Peer & Non Peer)Articlepeer-review

15 Citations (Scopus)

Abstract

Summary Hereditary haemolytic anaemia with basophilic stippling caused by pyrimidine 5′‐nucleotidase deficiency is described in three members of two unrelated Irish families. In one family, the disease was moderately severe and the patient's condition was improved by splenectomy. In the other family the haemolytic anaemia was well compensated. In neither family was there a marked elevation of reduced glutathione. The implications are that pyrimidine 5′‐nucleotidase deficiency is a heterogeneous disorder, both clinically and biochemically. In more severe forms splenectomy may be beneficial.

Original languageEnglish
Pages (from-to)27-34
Number of pages8
JournalClinical and Laboratory Haematology
Volume3
Issue number1
DOIs
Publication statusPublished - Mar 1981
Externally publishedYes

Keywords

  • hereditary haemolytic anaemia
  • red cell pyrimidine 5′‐nucleotidase deficiency
  • splenectomy

Fingerprint

Dive into the research topics of 'Hereditary haemolytic anaemia due to red cell pyrimidine 5‘‐nucleotidase deficiency in two Irish families with a note on the benefit of splenectomy'. Together they form a unique fingerprint.

Cite this