December_Group_August29: FA pg 79-89 - target99

[ArchivalUser]

mcardles-muscle phosphorylase
pompes-glucose 6 phosphatase
Hers hepatic phosphorylase
vongirkes-lysosomal Alpha 1-4 glucosidase
Anderson-??
plz. tell me if I'm wrong

[ArchivalUser]

guys,this group is doing great.....
encourage more question here as that is what is the tricky part in usmle.
well done john.we are proud of you for being so active

[ArchivalUser]

yes rt docritu..theer are 12 in total but impt are 6
type-1=Von gerke==>G6p deficiency
typeII=pompe's===>lysosomal aplha-i,4 glucosidase def
typeIII=cory's==>debranching enzyme def
TypeIV=Mcardle's=>muscle(skeletal) glycogen phosphorlysae def
typeV=her's============>hepatic ,, ,,
type VI=andersen's==>brabching enyzyme def

all-AUTOSOMAL RECESSIVE DIS(enzyme defects)

[ArchivalUser]

now autosomal dis
name as many as u remember

[ArchivalUser]

now autosomal dominant dis
name as many as u remember

[ArchivalUser]

what's energy source for liver in gluconeogenesis?

[ArchivalUser]

FAs

[ArchivalUser]

The following is the right order.....

type-1=Von gerke==>G6p deficiency
typeII=pompe's===>lysosomal aplha-i,4 glucosidase def
typeIII=cory's==>debranching enzyme def
type IV=andersen's==>branching enyzyme def
TypeV=Mcardle's=>muscle(skeletal) glycogen phosphorlysae def
typeVI=her's============>hepatic glycogen phosphorlysae def

[ArchivalUser]

I have mnemonic for this...

Very Poor CArbohydrate Metabolism Here--->

V P C A M H

[ArchivalUser]

oops sorry--yes mcardles is Type V and hers Type VI
and andersen type VI
thansk alot kashkala
juz typed how i had them on my mind..thanks for correction,appreciate it..