Paper I
2023 July (Supplementary) (2019 Scheme) · 100 marks · 180 min

Question

What is the most common RBC defect in Hereditary Spherocytosis.

Q181 marks

Answer

Deficiency/defect of the red cell membrane cytoskeletal protein spectrin (or its associated protein ankyrin), causing loss of membrane surface area relative to cell volume and producing the characteristic spherocyte shape.

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