Literature DB >> 2242432

Molecular and hematologic characterization of Scottish-Irish type (epsilon gamma delta beta)zero thalassemia.

R J Trent1, B G Williams, A Kearney, T Wilkinson, P C Harris.   

Abstract

The DNA deletion associated with an example of (epsilon gamma delta beta)zero thalassemia (Scottish-Irish type) was characterized. The deletion is approximately 205 kb in length and involves the epsilon, G gamma, A gamma, delta, and beta globin genes. The breakpoint is located 263 bp 3' to exon 3 of the beta globin gene. An LI (KpnI) repeat element approximately 320 bp in size is found at the 3' end of the novel DNA sequence. Different clinical phenotypes for three heterozygous neonates suggest that the deletion alone does not predict severity of (epsilon gamma delta beta)zero thalassemia at this age.

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Year:  1990        PMID: 2242432

Source DB:  PubMed          Journal:  Blood        ISSN: 0006-4971            Impact factor:   22.113


  3 in total

1.  A novel (epsilongammadeltabeta)(o)-thalassemia deletion associated with an alpha globin gene triplication leading to a severe transfusion dependent fetal thalassemic syndrome.

Authors:  Christian Rose; Julien Rossignol; Anne Lambilliotte; Sandrine Depret; Nathalie Le Metayer; Serge Pissard
Journal:  Haematologica       Date:  2009-03-13       Impact factor: 9.941

2.  Severe intrauterine anemia: a new form of epsilongammagammadeltabeta thalassemia presenting in utero in a Norwegian family.

Authors:  Anne Brantberg; Sturla H Eik-Nes; Nigel Roberts; Chris Fisher; William G Wood
Journal:  Haematologica       Date:  2009-06-22       Impact factor: 9.941

3.  Case Report: Clinical and Hematological Characteristics of εγδβ Thalassemia in an Italian Patient.

Authors:  Ilaria Fotzi; Francesco Pegoraro; Elena Chiocca; Tommaso Casini; Massimo Mogni; Marinella Veltroni; Claudio Favre
Journal:  Front Pediatr       Date:  2022-03-17       Impact factor: 3.418

  3 in total

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