Tab. 6. Mechanisms of intracellular accumulation of substances (Intracellular Accumulations or parenchymal dystrophies) 1. Normal cell 13 Protein mutation 0 Complex Soluble substrate products Enzyme (1) Abnormal metabolism. 2 Defect in protein folding, transport -X- 3 Lack of enzyme Fatty liver 4 Ingestion of indigestible materials CH Accumulation of abnormal proteins Complex substrate Lysosomal storage disease accumulation of endogenous materials Accumulation of exogenous materials 2. 3. 4.
Tab. 6. Mechanisms of intracellular accumulation of substances (Intracellular Accumulations or parenchymal dystrophies) 1. Normal cell 13 Protein mutation 0 Complex Soluble substrate products Enzyme (1) Abnormal metabolism. 2 Defect in protein folding, transport -X- 3 Lack of enzyme Fatty liver 4 Ingestion of indigestible materials CH Accumulation of abnormal proteins Complex substrate Lysosomal storage disease accumulation of endogenous materials Accumulation of exogenous materials 2. 3. 4.
Human Anatomy & Physiology (11th Edition)
11th Edition
ISBN:9780134580999
Author:Elaine N. Marieb, Katja N. Hoehn
Publisher:Elaine N. Marieb, Katja N. Hoehn
Chapter1: The Human Body: An Orientation
Section: Chapter Questions
Problem 1RQ: The correct sequence of levels forming the structural hierarchy is A. (a) organ, organ system,...
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Transcribed Image Text:Tab. 6. Mechanisms of intracellular accumulation of substances (Intracellular Accumulations or parenchymal dystrophies)
1.
Normal cell
Protein mutation
Complex
substrate
Soluble
products
Enzyme
Abnormal
metabolism
Defect in
protein
folding,
transport
-X->
Lack of
enzyme
Fatty liver
4
Ingestion of
indigestible
materials
Accumulation of
abnormal proteins
Complex
substrate
Lysosomal storage disease:
accumulation of
endogenous materials
Accumulation of
exogenous materials
12.
3.
4.
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