Literature DB >> 8166888

Hemoglobin D Ibadan-beta zero thalassemia: detection by neonatal screening and confirmation by electrospray-ionization mass spectrometry.

P A Lane1, H E Witkowska, A M Falick, M L Houston, J D McKinna.   

Abstract

We describe an infant with hemoglobin D Ibadan-beta zero thalassemia whose hemoglobinopathy was initially detected by neonatal screening. This previously undescribed condition was confirmed by family studies and by globin chain analysis by mass spectrometric techniques. The case illustrates the importance to neonatal screening programs of confirmatory testing and of linkage with reference laboratories capable of globin chain analysis. Hematologic studies at 36 months of age suggested that the presence of hemoglobin D Ibadan had no deleterious effect on this child with heterozygous beta zero thalassemia.

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Year:  1993        PMID: 8166888     DOI: 10.1002/ajh.2830440304

Source DB:  PubMed          Journal:  Am J Hematol        ISSN: 0361-8609            Impact factor:   10.047


  1 in total

1.  The splenic syndrome in individuals with sickle cell trait.

Authors:  Jessica Goodman; Kathryn Hassell; David Irwin; Ewa H Witkowski; Rachelle Nuss
Journal:  High Alt Med Biol       Date:  2014-12       Impact factor: 1.981

  1 in total

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