Cell Bio Diseases Word Scramble
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Question | Answer |
Tay Sach's Disease: Cellular/Molecular cause and key symptoms: | *Lysosome disease *Hesozamanadase A *Ganglioside GM2 *Cherry red macula |
Hurler Syndrome: Cellular/Molecular cause and key symptoms: | *Lysosome disease *Iduronidase *GAGs *Corneal clouding *Hepatosplenomegaly |
Hunter Syndrome: Cellular/Molecular cause and key symptoms: | *Lysosome disease *I2S enzyme *GAGs *Clear corneas *Hepatosplenomegaly |
Inclusion Cell Disease: Cellular/Molecular cause and key symptoms: | *Protein transport disease *Golgi-specific GlcNAc phosphotransferase *Acid hydrolases can't enter lysosome *M6P in golgi |
Alzheimer Disease: Cellular/Molecular cause and key symptoms: | *Protein misfolding disease *APP abnormally cleaved by secretase *Neurotoxic peptide *Neurofibullar tangle hyperphosphorylated tau *APP on chromosomes 21 (Downs) |
Zellweger Syndrome: Cellular/Molecular cause and key symptoms: | *Protein transport disease *Enzymes from ER can't enter peroxisome *No SKL tag *Profound hypotonia |
TSE: Cellular/Molecular cause and key symptoms: | *Prion Disease *Abnormal variant protein induces abnormal folding of normal protein. *PRPsc accumulates *Personality changes |
X-Linked Adrenoleukodystrophy: Cellular/Molecular cause and key symptoms: | *Membrane transport disease *VLCFAs cannot enter peroxisome *ABCD1 is mutated *Lipids accumulate |
Cystic Fibrosis: Cellular/Molecular cause and key symptoms: | *Membrane transport disease *CFTR misfolded/destroyed *Progressive lung disease *Pancreatic insufficiency |
Huntington's disease: Cellular/Molecular cause and key symptoms: | *Protein misfolding disease *Autosomal dominant *Polyglutamine expansion >40 copies (IT15) *Anticipation *Huntingtin aggretates in neurons *Personality changes, Chorea |
Gaucher's Disease: Cellular/Molecular cause and key symptoms: | *Lysosome disease *Glucocerebrosidase enzyme *Glucocerebroside accumulates *Characteristic macrophages *BONE PROBLEMS |
Leber's Hereditary Optic Neuropathy: Cellular/Molecular cause and key symptoms: | *Mitochondria disease *NADH dehydrogenase *Blindness in one eye, then other eye *Mitochondrial DNA from mom only |
Hereditary Spherocytosis: Cellular/Molecular cause and key symptoms: | *Cytoskeltal disease *Ankyrin 1 or Spectrin gene mutation *PM uncouples cytoskeleton *RBCs swell/lyse *Anemia/Pallor/Fatigue |
Familial Hypercholesterolemia: Cellular/Molecular cause and key symptoms: | *Receptor-mediated endocytosis disease *LDLR mutated (6 types) *LDL endocytosis disrupted *Xanthomas |
6 LDLR mutations | 1. Can't make LDLR in ER 2. Can't export LDLR from ER 3. Can't bind LDLR vesicle with PM 4. LDLR inactive on PM 5. LDLR binds without endocytosis 6. LDL-bound LDLR vesicle cannot bind endosome |
Pompe's Disease: Cellular/Molecular cause and key symptoms: | *Glycogen Storage Disease *a-1-4-Glucosidase *Glycogen accumulates in cells *Hypotonia *Cardiomegaly *RDS *Glycogen in tissues |
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chemicalpintobeans
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