医
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脾肿大、溶血
Congenital erythrocyte membrane disease (hereditary spherocytosis/elliptocytosis) is RBC membrane defect; hemolytic anemia/splenomegaly/gallstones.
Chronic hemolytic anemia; jaundice; splenomegaly; gallstones; aplastic crisis
Membrane protein (spectrin/ankyrin) mutation; autosomal dominant.
Folate; splenectomy if severe; cholecystectomy
Genetic counseling.
It is recommended to visit the hematology department; before the visit you may first book an appointment and connect with experts through this platform.
Warm reminder: The above information is provided for health education reference only and cannot replace professional medical diagnosis. If you have related symptoms, please seek care at a regular hospital in time.
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