Literature DB >> 6270945

A case of hemolytic anemia due to erythrocyte pyrimidine 5'-nucleotidase deficiency.

S Ozsoylu, A Gurgey.   

Abstract

A propositus, the offspring of a first-cousin marriage, was presented with severe hemolytic anemia, splenomegaly, jaundice, and growth retardation. Marked basophilic stippling of erythrocytes was shown by Wright's stain. Erythrocyte 5'-nucleotidase activity was found markedly decreased, whereas red blood cell glucose-6-phosphate dehydrogenase activity was elevated as the reduced glutathione level. His growth and anemia improved following splenectomy. His sister was also similarly affected.

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Year:  1981        PMID: 6270945     DOI: 10.1159/000207094

Source DB:  PubMed          Journal:  Acta Haematol        ISSN: 0001-5792            Impact factor:   2.195


  5 in total

1.  Splenectomy complicated by sustained extreme thrombocytosis and extensive portosplenomesenteric vein thrombosis in pyrimidine 5'-nucleotidase deficiency.

Authors:  Hassan A Al-Jafar; Ali Taqi; John Patrick Madda; Thamer A Abdullah
Journal:  BMJ Case Rep       Date:  2013-11-28

2.  Detection of pyrimidine 5'-nucleotidase deficiency using 1H- or 31P-nuclear magnetic resonance.

Authors:  T Kagimoto; K Shirono; T Higaki; T Oda; H Matsuzaki; K Nagata; T Nakaji; Y Morino; K Takatsuki
Journal:  Experientia       Date:  1986-01-15

3.  About pyrimidine 5'-nucleotidase deficiency.

Authors:  Sinasi Ozsoylu
Journal:  Turk J Haematol       Date:  2013-06-05       Impact factor: 1.831

4.  Recommendations regarding splenectomy in hereditary hemolytic anemias.

Authors:  Achille Iolascon; Immacolata Andolfo; Wilma Barcellini; Francesco Corcione; Loïc Garçon; Lucia De Franceschi; Claudio Pignata; Giovanna Graziadei; Dagmar Pospisilova; David C Rees; Mariane de Montalembert; Stefano Rivella; Antonella Gambale; Roberta Russo; Leticia Ribeiro; Jules Vives-Corrons; Patricia Aguilar Martinez; Antonis Kattamis; Beatrice Gulbis; Maria Domenica Cappellini; Irene Roberts; Hannah Tamary
Journal:  Haematologica       Date:  2017-05-26       Impact factor: 9.941

5.  Novel homozygous nonsense mutation in the P5'N-1 coding gene as an alternative cause for hereditary anemia with basophilic stippling.

Authors:  Martin Kirschner; Inga Rebecca Heinen; Steffen Koschmieder; Licinio Manco; Celeste Bento; Thomas Eggermann; Ingo Kurth; Edgar Jost; Tim H Brümmendorf; Roland Fuchs
Journal:  Clin Case Rep       Date:  2022-03-04
  5 in total

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