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Biochemistry Phospholipids, Glycolipids and their disorders 08bbb20f

Hunter syndrome is due to deficiency of -

A
Beta galactosidase
B
Sphingomyelinase
C
Iduronate Sulfatase
D
Hyaluronidase
High-Yield Explanation
Ans. is 'c' i.e., Induronate Sulfatase DiseaseDeficiencyInheritanceGM1 gangliosidosesBeta galactosidaseARMucopolySaccharidosesMPS I-Hurler syndromea-L-iduronidaseARMPS II-Hunter syndromeIduronate sulfataseXRMPS IIISanfilippo syndrome AHeparan sulfamidaseARSanfilippo syndrome BN-acetylglucosaminidaseSanfilippo syndrome CAcetyl-CoA: alphaglucosaminide acetyltransferaseSanfilippo syndrome DN-acetylglucosamine-6-sulfataseMPS IVMorquio syndrome AGalactose-6-sulfate sulfataseARMorquio syndrome BBeta-galactosidaseMPS VI - Maroteaux-Lamy syndromeN-acetylgalactosamine-4-sulfataseARMPS VII - Sly syndromeb-glucuronidaseARMPS IX - Natowicz syndromeHyaluronidaseAR

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