scholarly journals Detection of Compound Heterozygous Sickle Cell-b+ Thalassaemia in a Patient with Extreme Weakness, Mild Jaundice and Moderate Anaemia - A Case Report

Author(s):  
Subhash Chandra
2011 ◽  
Vol 31 (2) ◽  
pp. 130-133
Author(s):  
Bikash Shrestha ◽  
Kavita Karmacharya ◽  
Jasjit Singh ◽  
Jyoti Kotwal ◽  
Amit Devgan

Sickle cell disease is a type of hemoglobinopathy, which is fairly common in certain parts of the world. We would like to report an interesting case of a child who was labeled as sickle cell anemia but subsequently turned out to be a case of compound heterozygous sickle cell and thalassemia trait. Keywords: Sickle cell disease; haemoglobinopathy; thalassemia; hydroxyurea; globin; electrophoresis; HPLC DOI: 10.3126/jnps.v31i2.4414 J Nep Paedtr Soc 2010;31(2):130-133


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Author(s):  
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Author(s):  
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