A Rare Case of Hemoglobin Bart’s Hydrops Fetalis due to Uniparental Disomy of Chromosome 16

Hemoglobin (Hb) Bart’s hydrops fetalis is the most severe form of α-thalassemia and is usually inherited in an autosomal recessive manner. We report a case of Hb Bart’s hydrops fetalis due to uniparental disomy of chromosome 16. Antenatal screening showed a low maternal mean corpuscular volume (MCV)...

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Detalles Bibliográficos
Autores principales: Tan, Yin Ru, Tan, Hak Koon
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Elmer Press 2021
Materias:
Case Report
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8383697/
https://www.ncbi.nlm.nih.gov/pubmed/34434471
http://dx.doi.org/10.14740/jmc3693

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8383697/
https://www.ncbi.nlm.nih.gov/pubmed/34434471
http://dx.doi.org/10.14740/jmc3693

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