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Alpha thalassemia allelic frequency in Lebanon
Pediatric Blood & Cancer, 2014BackgroundHemoglobinopathies are the most common reported monogenic disorders worldwide. It is well established that Mediterranean and Arab countries are high risk areas for thalassemia in general, and for alpha thalassemia in particular. Reports of alpha thalassemia gene mutations from the Lebanese population are limited.ProcedureWe investigated the ...
Chantal, Farra +8 more
openaire +2 more sources
Alpha-thalassemia in Thailand.
Hemoglobin, 1989The alpha-thalassemia syndromes are remarkable both for their phenotypic diversity and for their different clinical severity. They are associated with variable degrees of alpha-chain deficits; the clinical manifestations range from asymptomatic cases with normal hematologic findings to the totally lethal Hb Bart's hydrops fetalis syndrome.
P, Winichagoon +4 more
openaire +1 more source
Alpha-Thalassemia: Diversity of Clinical Phenotypes and Update on the Treatment
Thalassemia Reports, 2022Duantida Songdej +2 more
exaly
Successful preimplantation genetic diagnosis for alpha- and beta-thalassemia in China
Prenatal Diagnosis, 2006Fang Cong, Liang Xiao-Yan, Cong Fang
exaly
Distribution of alpha-thalassemia mutations in Iranian population
Hematology, 2015Mohamad Moghadam +2 more
exaly