Please use this identifier to cite or link to this item: http://hdl.handle.net/123456789/23248
Title: Human hemoglobin G-Makassar variant masquerading as sickle cell anemia
Authors: Mohamad, A.S.
Hamzah, R.
Selvaratnam, V.
Yegapan, S.
Sathar, J.
Keywords: Hemoglobin G-Makassar
electrophoresis
beta thalassemia
DNA analysis
sickle cell disease
Issue Date: Sep-2018
Publisher: Page Press Publications
Citation: Mohamad, A. S., Hamzah, R., Selvaratnam, V., Yegapan, S., & Sathar, J. (2018). Human hemoglobin G-Makassar variant masquerading as sickle cell anemia. Hematology Reports, 10(3), 92–95.
Abstract: Human hemoglobin of G-Makassar variant has been reported very rarely with Beta Thalassemia. In year 1969 Hb GMakassar was first identified in Makassar, Sulawesi (Celebes), Republic of Indonesia. The disease was first published in 1969 and 33 years later it has been reported at a family of Thailand origin. We report a 45-yearold Malay man who was investigated for anemia and thrombocytopenia then diagnosed with Hb G-Makassar. This finding describes as a new Hemoglobin GMakassar discovered in Malaysia after 14 years diagnosed in Thailand.
Description: This is an open access article distributed under the terms of the Creative Commons CC-BY license. This article index by Scopus
URI: https://doi.org/10.4081/hr.2018.7210
https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6176384/
http://ir.unikl.edu.my/jspui/handle/123456789/23248
ISSN: 20388322
Appears in Collections:Journal Articles

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