Hereditary elliptocytosis

Hereditary elliptocytosis (HE) is a rare clinically and genetically heterogeneous disorder of the red cell membrane characterized by manifestations ranging from mild to severe transfusion-dependent hemolytic anemia but with the majority of patients being asymptomatic.

Hepatitis

Inflammation of the liver.


Total: 1

                      


(per page)
PMID (PMCID)
6727059
FEMALE Adult
A case of hereditary elliptocytosis associated with constitutional indocyanine green excretory defect.
Taketazu F, Sanada I, Ngamatsu N, Mukai R, Suetomo Y, Toyoda N, Takada M, Hida K, Kubota K, Maezawa M, et al..
Jpn J Med. 1984;23(2):139-43.
A 24-year-old woman was diagnosed as having hereditary elliptocytosis and post-transfusion hepatitis.