Concept explainers
To determine: The age at which Cori’s disease is typically noticed.
Concept introduction:
Glycogen storage disease type III (GSD III) or Cori’s disease is an inherited rare disorder. It is caused by deficient activity of glycogen debranching enzyme that is amylo-1, 6-glucosidase. Deficiency of this enzyme, results in glycogen accumulation in tissues.
To explain: The clinical symptoms of Cori’s disease.
Concept introduction:
Glycogen storage disease type III (GSD III) or Cori’s disease is an inherited rare disorder. It is caused by lacking activity of glycogen debranching enzyme that is amylo-1, 6-glucosidase. Deficiency of this enzyme, results in glycogen accumulation in tissues.
To explain: How to diagnosis Cori’s disease.
Concept introduction:
Glycogen storage disease type III (GSD III) or Cori’s disease is an inherited rare disorder. It is caused by lacking activity of glycogen debranching enzyme that is amylo-1, 6-glucosidase. Deficiency of this enzyme, results in glycogen accumulation in tissues.
To explain: How Cori’s disease is treated.
Concept introduction:
Glycogen storage disease type III (GSD III) or Cori’s disease is an inherited rare disorder. It is caused by lacking activity of glycogen debranching enzyme that is amylo-1, 6-glucosidase. Deficiency of this enzyme, results in glycogen accumulation in tissues.
To explain: The variant forms of Cori’s disease, and the genetic basis for the variation.
Concept introduction:
Glycogen storage disease type III (GSD III) or Cori’s disease is an inherited rare disorder. It is caused by lacking activity of glycogen debranching enzyme that is amylo-1, 6-glucosidase. Deficiency of this enzyme, results in glycogen accumulation in tissues.
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