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The first report of a homozygous codons 9/10 (+T) ß-thalassemia mutation in a Turkish patient.
Unal, Sule; Chui, David H K; Luo, Hong-Yuan; Okur, Hamza; Oymak, Yesim; Gumruk, Fatma.
Afiliação
  • Unal S; Division of Pediatric Hematology, Hacettepe University , Ankara , Turkey.
Hemoglobin ; 39(1): 66-8, 2015.
Article em En | MEDLINE | ID: mdl-25572182
ABSTRACT
For the first time in Turkey, we report a thalassemic patient with a homozygous codons 9/10 (+T) genotype. Currently, the patient is 3 years and 2 months old and received an initial transfusion at the age of 18 months. After being alloimmunized following this transfusion, he required frequent transfusions, every week to every other week. Although alloimmunization was controlled after methyl-prednisolone, intravenous immunoglobulin, plasmapheresis and rituximab, the transfusion requirements continued related to hypersplenism. Subsequent to splenectomy, transfusion requirements disappeared with average hemoglobin (Hb) levels around 11.0 g/dL. The mother underwent prenatal diagnosis (PND) when she became pregnant for the third time; this revealed a heterozygous codons 9/10 fetus.
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Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Talassemia beta / Globinas beta Limite: Child, preschool / Female / Humans / Infant / Male / Pregnancy País/Região como assunto: Asia Idioma: En Revista: Hemoglobin Ano de publicação: 2015 Tipo de documento: Article País de afiliação: Turquia

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Talassemia beta / Globinas beta Limite: Child, preschool / Female / Humans / Infant / Male / Pregnancy País/Região como assunto: Asia Idioma: En Revista: Hemoglobin Ano de publicação: 2015 Tipo de documento: Article País de afiliação: Turquia