sample table entry via PDF cut paste
|
Tay-Sachs disease Krabbe’s disease |
||||
|
Peripheral neuropathy, developmental delay, optic atrophy, globoid cells |
Galactocerebrosidase |
Galactocerebroside |
AR |
|
|
Metachromatic leukodystrophy |
Central and peripheral demyelination with ataxia, dementia |
Arylsulfatase A |
Cerebroside sulfate |
AR |
|
Mucopolysaccharidoses |
||||
|
Hurler’s syndrome |
Developmental delay, gargoylism, airway obstruction, corneal clouding, hepatosplenomegaly |
α-L-iduronidase |
Heparan sulfate, dermatan sulfate |
AR |
|
Hunter’s syndrome |
Progressive neurodegeneration,
developmental delay, cherry-red spot on macula, lysosomes with onion skin, no hepatosplenomegaly (vs. Niemann-Pick)
Hexosaminidase A GM2ganglioside AR
Mild Hurler’s + aggressive behavior, no Iduronate sulfatase Heparan sulfate, XR
Customer support service by UserEcho