Case series of homozygous and compound heterozygosity of Hb Malay, the diagnostic features and transfusion requirements

Case series of homozygous and compound heterozygosity of Hb Malay, the diagnostic features and transfusion requirements

Hb Malay was first described in 1989 following an investigation of anaemia in a 22-year-old Malay gentleman who was homozygous for this b chain variant. This Hb variant is caused by AAC à AGC mutation at codon 19 of the b globin gene resulting in the substitution of serine for asparagine [1]. The mu...

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Bibliographic Details
Main Authors: Amran, Hanizah Salwa, Sarijan, Nurimatussolehah, Sathar, Jameela, Md Noor, Sabariah
Format: Article
Language:English
Published: Advanced Medical and Dental Institute (AMDI) 2017
Online Access:http://psasir.upm.edu.my/id/eprint/61055/
http://psasir.upm.edu.my/id/eprint/61055/1/Case%20series%20of%20homozygous%20and%20compound%20heterozygosity%20of%20Hb%20Malay%2C%20the%20diagnostic%20features%20and%20transfusion%20requirements.pdf

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