Journal article
α‐Thalassemia: Hb H Disease and Hb Barts Hydrops Fetalis
Abstract
alpha-Thalassemia mutations are one of the most common mutations of man, and they cause Hb H disease and Hb Barts hydrops fetalis. Hb H disease is not necessarily a benign disorder as has been generally thought. Furthermore, in southern China and in Southeast Asia, there are 2-3 times more fetuses afflicted with the invariably fatal Hb Barts hydrops fetalis than with the beta-thalassemia major or intermedia. These findings underscore the public …
Authors
Chui DHK
Journal
Annals of the New York Academy of Sciences, Vol. 1054, No. 1, pp. 25–32
Publisher
Wiley
Publication Date
11 2005
DOI
10.1196/annals.1345.004
ISSN
0077-8923
Fields of Research (FoR)
Sustainable Development Goals (SDG)
Medical Subject Headings (MeSH)
Asia, SoutheasternChinaFemaleFetal DeathFetal DiseasesForecastingGene FrequencyGenotypeGlobinsHealth EducationHemoglobins, AbnormalHumansHydrops FetalisInfant, NewbornInternational CooperationMaleMutationPregnancyPregnancy Complications, HematologicPregnancy OutcomePrenatal DiagnosisResearchRiskSequence DeletionStillbirthalpha-Thalassemia