Nonimmune hydrops fetalis due to autosomal recessive hereditary spherocytosis

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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Bibliographic Details
Main Authors: Dawn M. Hannah, Terry B. Tressler, Claudia D. Taboada
Format: Article
Language:English
Published: Elsevier 2017-10-01
Series:Case Reports in Women's Health
Subjects:
Hereditary spherocytosis
Fetal anemia
Nonimmune hydrops fetalis
Autosomal recessive
α-Spectrin
SPTA1
Online Access:http://www.sciencedirect.com/science/article/pii/S2214911217300577

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http://www.sciencedirect.com/science/article/pii/S2214911217300577

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