Literature DB >> 16114185

The first case of Hb E-Saskatoon associated with Hb Lepore-Baltimore found in Spain.

Paloma Ropero1, Maria José Murga, Fernando A González, Marta Polo, Celina Benavente, María Salvador, Ana Villegas.   

Abstract

Hb E-Saskatoon [beta22(B4)Glu-->Lys] does not cause any clinical symptoms in the heterozygous state. The homozygous state shows moderate phenotype expression. It has also been detected in association with beta-thalassemia. We present the first case of Hb E-Saskatoon associated with Hb Lepore-Baltimore. This unusual combination of mutations does not aggravate the clinical picture, as only microcytosis and hypochromia have been observed. Hb E-Saskatoon can only be correctly characterized by ion exchange high performance liquid chromatography (HPLC) or by DNA sequencing.

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Year:  2005        PMID: 16114185     DOI: 10.1081/hem-200066321

Source DB:  PubMed          Journal:  Hemoglobin        ISSN: 0363-0269            Impact factor:   0.849


  2 in total

1.  Prenatal Diagnosis of HbE-β-Thalassemia: Experience of a Center in Western India.

Authors:  Roshan Colah; Anita Nadkarni; Ajit Gorakshakar; Pratibha Sawant; Khushnooma Italia; Dipti Upadhye; Harshali Gaikwad; Kanjaksha Ghosh
Journal:  Indian J Hematol Blood Transfus       Date:  2017-09-04       Impact factor: 0.900

2.  Corpuscular Haemolytic Anaemias - Lepore Haemoglobinopathy.

Authors:  Iulia Tudorascu; Simona Neamtu; Liliana Stanca; Mirela Siminel; Lorena Dijmarescu; Magdalena Manolea; Liliana Novac; Elis Pirgaru; Suzana Danoiu
Journal:  Curr Health Sci J       Date:  2014-12-14
  2 in total

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