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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 |
Files in This Item:
File | Description | Size | Format | |
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Human hemoglobin G-Makassar variant masquerading as sickle cell anemia.pdf | 226.82 kB | Adobe PDF | View/Open |
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