Literature DB >> 7803273

Red cell membrane protein abnormalities in hereditary spherocytosis in Brazil.

S T Saad1, F F Costa, D L Vicentim, T S Salles, P H Pranke.   

Abstract

We studied 14 kindred and nine unrelated patients from southeastern Brazil with the typical form of hereditary spherocytosis. Diagnosis was made on the basis of clinical features, presence of spherocytes on the peripheral blood smears and an abnormal osmotic fragility test. By densitometric tracing of SDS-PAGE stained by Coomassie blue, we detected isolated deficiency of spectrin in 39% of our patients, combined spectrin and ankyrin deficiency in 13%, and deficiency of band 3 in 13%. One of our patients presented ankyrin deficiency without spectrin reduction. Our data suggest that, despite ethnic differences among the Brazilian and European or North-American populations, these biochemical abnormalities in HS patients may be similar.

Entities:  

Mesh:

Substances:

Year:  1994        PMID: 7803273     DOI: 10.1111/j.1365-2141.1994.tb05021.x

Source DB:  PubMed          Journal:  Br J Haematol        ISSN: 0007-1048            Impact factor:   6.998


  2 in total

1.  A nonsense mutation in the erythrocyte band 3 gene associated with decreased mRNA accumulation in a kindred with dominant hereditary spherocytosis.

Authors:  P B Jenkins; G K Abou-Alfa; D Dhermy; E Bursaux; C Féo; A L Scarpa; S E Lux; M Garbarz; B G Forget; P G Gallagher
Journal:  J Clin Invest       Date:  1996-01-15       Impact factor: 14.808

2.  Effect of primary lesions in cytoskeleton proteins on red cell membrane stability in patients with hereditary spherocytosis.

Authors:  Cristina Vercellati; Anna Paola Marcello; Bruno Fattizzo; Anna Zaninoni; Agostino Seresini; Wilma Barcellini; Paola Bianchi; Elisa Fermo
Journal:  Front Physiol       Date:  2022-08-12       Impact factor: 4.755

  2 in total

北京卡尤迪生物科技股份有限公司 © 2022-2023.