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Medicine G.I.T 3c724092

True about Crigger Najjar type II syndrome is-

A
Diglucuronide deficiency
B
Recessive trait
C
Kemicterus is seen
D
Phenobarbitone not useful
High-Yield Explanation
Crigler najar type 2 is an autosomal recessive condition in which there is decrease in glucuronyl transferase, Treatment includes phenobarbital, phototherapy or liver transplant. Kernicterus is seen in type 1 not type 2. Reference: Davidson, 23rd edition, page 860

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