Please use this identifier to cite or link to this item: http://cmuir.cmu.ac.th/jspui/handle/6653943832/77076
Title: Coinherited Hemoglobin H/Constant Spring Disease and Heterozygous Hemoglobin Tak Causing Severe Hemolytic Anemia in a Thai Boy
Authors: Chane Choed-Amphai
Arunee Phusua
Chupong Ittiwut
Pimlak Charoenkwan
Kanya Suphapeetiporn
Vorasuk Shotelersuk
Authors: Chane Choed-Amphai
Arunee Phusua
Chupong Ittiwut
Pimlak Charoenkwan
Kanya Suphapeetiporn
Vorasuk Shotelersuk
Keywords: Medicine
Issue Date: 1-Jul-2021
Abstract: Hemoglobin (Hb) H/Constant Spring disease is a common nondeletional Hb H disease, typically causing a more severe phenotype than the deletional Hb H disease counterpart. Hb Tak, resulting from a dinucleotide insertion (+AC) at codon 146 of beta-globin gene, has an increased oxygen affinity and usually presents with polycythemia. We studied a case of a 4-year-old Thai boy with a severe, early-onset anemia. To our knowledge, he is the first reported patient with Hb H/Constant Spring disease and heterozygous Hb Tak. Trio-whole-exome sequencing does not identify other genetic variants that may contribute to the severity of anemia. The observation suggests that coinherited Hb H/Constant Spring and heterozygous Hb Tak lead to severe hemolytic anemia.
URI: https://www.scopus.com/inward/record.uri?partnerID=HzOxMe3b&scp=85109037002&origin=inward
http://cmuir.cmu.ac.th/jspui/handle/6653943832/77076
ISSN: 15363678
10774114
Appears in Collections:CMUL: Journal Articles

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