Recurrent acute splenic sequestration crisis due to interacting genetic defects: hemoglobin SC disease and hereditary spherocytosis.

Warkentin, T E

Recurrent acute splenic sequestration crisis due to interacting genetic defects: hemoglobin SC disease and hereditary spherocytosis. [electronic resource] - Blood Jan 1990 - 266-70 p. digital

Publication Type: Case Reports; Journal Article; Research Support, U.S. Gov't, P.H.S.

0006-4971


Anemia, Sickle Cell--complications
Erythrocyte Deformability
Erythrocyte Membrane--physiology
Hemoglobin SC Disease--complications
Humans
Male
Spectrin--deficiency
Spherocytosis, Hereditary--complications
Splenic Diseases--complications