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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...
| Autores principales: | , , |
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| Formato: | Online Artículo Texto |
| Lenguaje: | English |
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Elsevier
2017
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| 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 |