spherocytosis

n.

球形红细胞（贫血）症；

Hereditary spherocytosis associated with deletion of human erythrocyte ankyrin gene on chromosome 8
Hereditary spherocytosis--defects in proteins that connect the membrane skeleton to the lipid bilayer
Hereditary spherocytosis, thrombocytosis, and chronic pulmonary emboli: A case report and review of the literature
Partial deficiency of erythrocyte spectrin in hereditary spherocytosis.
Fine structure of the red pulp of the spleen in hereditary spherocytosis
Guidelines for the diagnosis and management of hereditary spherocytosis--2011 update.
Ankyrin-1 mutations are a major cause of dominant and recessive hereditary spherocytosis.
PARENTAL MOSAICISM FOR ANKYRIN-1 MUTATIONS IN TWO FAMILIES WITH HEREDITARY SPHEROCYTOSIS (HS)
Characterization of the underlying molecular defect in hereditary spherocytosis associated with spectrin deficiency (Abstract #1856)
Coinheritance of Gilbert syndrome increases the risk for developing gallstones in patients with hereditary spherocytosis.