Hemoglobin Alpha Chain Variant Zara Associated With Familial Asymptomatic Hypoxemia

Numerous hemoglobin (Hb) gene mutations have been identified, leading to a spectrum of phenotypes ranging from asymptomatic carrier states to complicated hemolytic anemias. We report a rare case of asymptomatic hypoxemia in a father and his teenage daughter both of whom were found to be carriers of...

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Detalles Bibliográficos
Autores principales: Pasquarella, Anthony, Miller, Erin, Wong, Edward C.C., Ito, Masamichi, Braunstein, Marc J.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Elmer Press 2022
Materias:
Case Report
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9635801/
https://www.ncbi.nlm.nih.gov/pubmed/36406831
http://dx.doi.org/10.14740/jh1028

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9635801/
https://www.ncbi.nlm.nih.gov/pubmed/36406831
http://dx.doi.org/10.14740/jh1028

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