Compound Heterozygous Hemoglobin Minneapolis-Laos and Codon 41/42 (-TTCT) in a Thai Female Adult: A Case Report and Literature Review.

doi:10.1080/03630269.2026.2684611

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Article

Compound Heterozygous Hemoglobin Minneapolis-Laos and Codon 41/42 (-TTCT) in a Thai Female Adult: A Case Report and Literature Review.

Hemoglobin - 1 Jul 2026

Preechathaveekid Sitanun, Rungjirajittranon Tarinee, Chanpo Nuttiruetai, Dujjawan Boonyanuch, Hantaweepant Chattree

Abstract excerpt

Thalassemia is a prevalent genetic disorder in Southeast Asia. The Hemoglobin Minneapolis-Laos variant is very rarely reported with only two previously published reports that profile a total of three patients. Here, we present the first reported case of compound heterozygous β zero (β0)-thalassemia and Hemoglobin Minneapolis-Laos in a 46-year-old Thai female. She presented at Siriraj Hospital (Bangkok, Thailand)...

Topics

Humans
Female
Hemoglobins, Abnormal
Middle Aged
Heterozygote
Thailand
beta-Thalassemia
Codon
Mutation
beta-Globins

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PMID: 42272137
DOI: 10.1080/03630269.2026.2684611

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PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 30 Aug 2026.

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