Nonimmune hydrops fetalis due to autosomal recessive hereditary spherocytosis

• Main Authors: Dawn M. Hannah (Author), Terry B. Tressler (Author), Claudia D. Taboada (Author)
• Formato: Livro
• Publicado em: Elsevier, 2017-10-01T00:00:00Z.
• Assuntos: article
• Acesso em linha: Connect to this object online.

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...