Literature DB >> 7149173

The pyropoikilocytosis-elliptocytosis syndrome in a black South African infant: clinical and hematological features.

L G MacDougall, G Moodley, M Quirk.   

Abstract

A black infant presented in the newborn period with severe red cell fragmentation, pyknocytosis, and hemolysis necessitating repeated exchange transfusions. Exposure of the red cells to 45 degrees C in vitro caused membrane budding, fragmentation, and sphering similar to that described in pyropoikilocytosis. By 12 months of age the clinical and hematologic picture had evolved to one of a compensated hemolytic disorder with elliptocytosis, but the degree of abnormal thermal sensitivity remained unchanged. Osmotic fragility and authohemolysis tests gave results intermediate between hereditary elliptocytosis and hereditary pyropoikilocytosis. It appears that there is considerable heterogeneity within the red cell membrane disorders exhibiting altered thermal sensitivity.

Entities:  

Mesh:

Year:  1982        PMID: 7149173

Source DB:  PubMed          Journal:  Am J Pediatr Hematol Oncol        ISSN: 0192-8562


  3 in total

Review 1.  Erythrocyte disorders in the perinatal period.

Authors:  Laurie A Steiner; Patrick G Gallagher
Journal:  Semin Perinatol       Date:  2007-08       Impact factor: 3.300

2.  Defective binding of spectrin to ankyrin in a kindred with recessively inherited hereditary elliptocytosis.

Authors:  S S Zail; T L Coetzer
Journal:  J Clin Invest       Date:  1984-09       Impact factor: 14.808

3.  Modulation of erythrocyte membrane mechanical stability by 2,3-diphosphoglycerate in the neonatal poikilocytosis/elliptocytosis syndrome.

Authors:  W C Mentzer; T A Iarocci; N Mohandas; P A Lane; B Smith; J Lazerson; T Hays
Journal:  J Clin Invest       Date:  1987-03       Impact factor: 14.808

  3 in total

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