Lysosomal disorders.txt

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Author:
UCFCOMcd
ID:
32379
Filename:
Lysosomal disorders.txt
Updated:
2010-09-02 00:22:08
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HB1 exam
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Lysosomal storage disorders
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  1. Lysosomal storage disorders
    Result in a mutation in the chain responsible for degrading gangliosides (glycolipids), act through GM1 Tay Sach, Karbbes, Gaucher, Neimann Pick, Fabry's--- al related to
  2. Tay Sachs
    *seen most often, deficient hexosaminidase A, accumulation of GM2 ganglioside substrate in tissue and nerve cells, cherry red spots in their eyes, unsteady gait *difference in TS and NP is hepatosplenomegaly, increased incidence in Ashkenai Jews
  3. Krabbe's disease
    deficienct in galactorcerebrosidase (mutation of GALC gene), accmulation of unmetabolized lipids, affects's nerves myelin sheath, peripheral neuropathy, developmental delay, generally fatal before age 2
  4. Gaucher's disease
    *most common, MISSING THE ENZYME glucocerebrosidase, accumulation of glucocerebrosides, the last step before removal of the final sugar from ceramide hepatosplenomegaly and neurogenerative disease and skeletal deterioration *developed exogenous B-glucosidase to successfully target lysosomes of macrophages using mannose receptor
  5. Neimann Pick syndrome
    defect in sphingomyelinasem accumulation of sphingomyelin in brain and RBS--> "foam cells" cherry red spot, mental retardation, spasticity, seizures, hepatosplenomegaly * ashkenzai jews
  6. Fabry's disease
    deficeint in alpha-galactose A accumulation of ceramide or alpha-galactosidase A *proteinuria, vertigo, small red raised bumps of scrotum (angiokeratoma), peripheral neuropathy * X-linked recessive trait, treatable with recombinant enzyme therapy alpha-galactose A
  7. Mucopolysaccharidoses Enzyme Proteoglycan accumulation
    Hunter's, Hurler's, Morqoi's, *Diagnosed by GAG chains in the urine, Products are secreted in urine
  8. Hunter's
    iduronic sulfatase, Heparan sulfate and dermatan sulfate, no corneal clouding
  9. Hunter's
    • alpha iduronase Heparan sulfate and dermatan sulfate, corneal clouding
    • Morqoi's A
    • galactose-6-sulfatase, keratan sulfate
  10. Morqoi's B,
    B-galactosidase, kertan sulfate

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