منابع مشابه
α-Thalassemia with Haemoglobin Adana mutation: prenatal diagnosis.
Thalassaemia carriers are common in the Asian region including Malaysia. Asymptomatic patients can be undiagnosed until they present for their antenatal visits. Devastating obstetric outcome may further complicate the pregnancy if both parents are thalassaemia carriers leading to hydrophic fetus due to haemoglobin Bart's disease. However in certain cases where unexplained hydrops fetalis occur ...
متن کاملCompound Heterozygous Beta Thalassemia with Heredietary Persistence of Fetal Haemoglobin: A Rare Haematological Combination and Different Spectrum of Thalassemia
5 year old male child presented with progressive abdominal distention, pallor, and growth failure since the age of 9 months. The foe did not respond to hematinic and required one blood transfusion for anemia. Liver and spleen were enlarged on abdominal exam. Peripheral smear showed features of haemolytic anemia and neonatal red blood cells. HPLC studies of patient revealed that father was a car...
متن کاملGrowth Status and Serum Zinc Level in Patients with Haemoglobin –E-β Thalassemia
Background: HbE β thalassemia is a major congenital hematological disease of Bangladesh. These patients have poor growth and delayed maturation mainly due to iron overload but zinc deficiency also has been suggested as a contributing
متن کاملReport of haemoglobin J-Toronto and alpha thalassemia in a family from North of Iran.
We report of an Iranian family with history of a rare haemoglobin variant, Haemoglobin J associated with alpha thalassemia, discovered while performing premarital thalassemia screening. In the present study we report the first case of haemoglobin J-Toronto [alpha 5 (A3) Ala > Asp] on -globin gene, found in a 16-year-old female from Mazandaran Province, North of Iran. Further investigation chara...
متن کاملEvaluation of an automatic HPLC analyser for thalassemia and haemoglobin variants screening
In this paper the authors report the evolution of a new automatic HPLC analyser for screening haemoglobinopathies. HbA(2) and F determinations are accurate and reproducible. The analysis time is short (6.5 min) and there is a good separation between the HbA(2) values of beta-thalassemia carriers from normals and alpha-thalassemia carriers, with no overlap between these groups. In addition, the ...
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ژورنال
عنوان ژورنال: Journal of Dr. NTR University of Health Sciences
سال: 2014
ISSN: 2277-8632
DOI: 10.4103/2277-8632.146672