Hexokinase deficiency

A rare, autosomal recessive, inherited disorder caused by mutation of the HK1 gene. It is characterized by the early-onset of severe, non-spherocytic hemolytic anemia.

Disease Alternative Name

hk1 deficiency
erythrocyte hexokinase deficiency
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Hyderabad
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BHASKARA HOSPITAL

OBSTETRICIAN &GYNECOLOGIST

Kakatiya Medical College

M.D ( OB&GY )

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