Nonimmune hydrops fetalis due to autosomal recessive hereditary spherocytosis

BACKGROUND: Hereditary spherocytosis is the most common form of inherited hemolytic anemia and is characterized by a structural defect in the RBC membrane. The disorder is commonly inherited in an autosomal dominant fashion and leads to a mild to moderate anemia. The autosomal recessive form of here...

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Detalles Bibliográficos
Autores principales: Hannah, Dawn M., Tressler, Terry B., Taboada, Claudia D.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Elsevier 2017
Materias:
Article
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5842958/
https://www.ncbi.nlm.nih.gov/pubmed/29594000
http://dx.doi.org/10.1016/j.crwh.2017.09.003

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5842958/
https://www.ncbi.nlm.nih.gov/pubmed/29594000
http://dx.doi.org/10.1016/j.crwh.2017.09.003

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