Article

A Rare Hemoglobinopathy Duo: Hb ADANA x Hb SEA in a One-Year-Old Patient

2023-09-06

Abstract excerpt

Female thalassemia carriers are often symptom-free until their prenatal visit, discovering their fetus has hydrops fetalis. However, a single alpha-thalassemia gene mutation doesn’t cause this. It requires an additional mutation from both parents, impacting the fetus’s genotype and phenotype. Here, we present a case of a one-year-old girl with an uncommon alpha-thalassemia type. Genetic testing revealed the mother...

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Literature Corpus work: 3ab7d99e-a6b9-54b6-8a17-7d2f2e2db1e2
DOI: 10.22541/au.169398727.72967647/v1

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