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The First Thai Case of Nondeletional HbH Disease Caused by Compound Heterozygosity for α-Thalassemia-1 Chiang Rai (--CR) Type Deletion with Hb Constant Spring.

Hemoglobin - 1 Jul 2024

Songdej Duantida, Kadegasem Praguywan, Sirachainan Nongnuch, Ruengdit Chedtapak, Punyamung Manoo, Pornprasert Sakorn

Abstract excerpt

Hemoglobin (Hb) H disease presents a wide range of clinical phenotypes, from asymptomatic to severe forms, depending on significant genetic heterogeneity. This is the first report of clinical and hematological features of the nondeletional HbH disease caused by --CR/αCSα. A baby was born to a father and a mother with --CR and αCSα carriers, respectively. She had severe symptomatic hypochromic microcytic anemia at...

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alpha-Thalassemia
Anemia, Hypochromic
Electrophoresis, Capillary
Erythrocyte Indices
Hemoglobin H

Methodology Data sources Editorial policy Privacy About Contact Helena Bioinformatics

Hemoglobins, Abnormal

Southeast Asian People

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PMID: 39177110
DOI: 10.1080/03630269.2024.2388661

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PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 1 Sept 2026.

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