Literature DB >> 2496567

Hydrops fetalis due to homozygosity for alpha-thalassemia-1, -(alpha)-20.5 kb: the first observation in a Turkish family.

A Gurgey1, C Altay, M S Beksaç, R Bhattacharya, F Kutlar, T H Huisman.   

Abstract

We report data on a fetus with hydrops fetalis due to a homozygosity for alpha-thalassemia-1, type -(alpha)-20.5 kb; this is the first reported case in a Turkish family. Characterization of the abnormality was based on data from family studies and from alpha-globin gene mapping of the DNA from the parents.

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Year:  1989        PMID: 2496567     DOI: 10.1159/000205553

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


  4 in total

1.  Homozygosity for the Mediterranean a-thalassemic deletion (hemoglobin Barts hydrops fetalis).

Authors:  Nasir A S Al-Allawi; Maida Y Shamdeen; Najeeb S Rasheed
Journal:  Ann Saudi Med       Date:  2010 Mar-Apr       Impact factor: 1.526

2.  The Hematological and Molecular Spectrum of α-Thalassemias in Turkey: The Hacettepe Experience.

Authors:  Şule Ünal; Fatma Gümrük
Journal:  Turk J Haematol       Date:  2015-06       Impact factor: 1.831

3.  A Case of Nonimmune Hydrops Fetalis Caused by Homozygous α-Thalassemia.

Authors:  Melek Akar; Dilek Dilli; Uğur Dilmen
Journal:  Turk J Haematol       Date:  2013-03-05       Impact factor: 1.831

4.  Hemoglobin H Disease in Turkey: Experience from Eight Centers.

Authors:  Selma Ünal; Gönül Oktay; Can Acıpayam; Gül İlhan; Edip Gali; Tiraje Celkan; Ali Bay; Barış Malbora; Nejat Akar; Yeşim Oymak; Tayfur Toptaş
Journal:  Turk J Haematol       Date:  2015-08-06       Impact factor: 1.831

  4 in total

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