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Homozygosity for the Mediterranean α-thalassemic deletion (hemoglobin Barts hydrops fetalis)
Hemoglobin Barts hydrops fetalis syndrome is the most severe and generally fatal clinical phenotype of α-thalassemia. We diagnosed a fetus at 23-weeks gestation with having hydrops fetalis, by ultrasound. At 32 weeks, intrauterine death was detected. Molecular studies revealed that the fetus had the...
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| Main Authors: | , , |
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| Formáid: | Artigo |
| Teanga: | Inglês |
| Foilsithe: |
Medknow Publications
2010
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| Ábhair: | |
| Rochtain Ar Líne: | https://ncbi.nlm.nih.gov/pmc/articles/PMC2855068/ https://ncbi.nlm.nih.gov/pubmed/20220267 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.4103/0256-4947.60523 |
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