Glycogen storage disease type III causes: Difference between revisions
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{{Glycogen storage disease type III}} | {{Glycogen storage disease type III}} | ||
{{CMG}}; {{AE}} | {{CMG}}; {{AE}} {{Anmol}} | ||
==Overview== | ==Overview== | ||
Glycogen storage disease type 3 is an [[autosomal recessive]] disorder. Glycogen storage disease type 3 is caused by the deficiency of the glycogen debranching (GDE) enzyme. [[AGL]] [[gene mutation]] responsible for the glycogen debranching (GDE) enzyme deficiency is located on [[chromosome]] 1p21. | |||
==Causes== | ==Causes== | ||
*Glycogen storage disease type 3 is an [[autosomal recessive]] disorder. | *Glycogen storage disease type 3 is an [[autosomal recessive]] disorder. | ||
*Glycogen storage disease type 3 is caused by the deficiency of the glycogen debranching (GDE) enzyme. [[AGL]] [[gene mutation]] responsible for the glycogen debranching (GDE) enzyme deficiency is located on [[chromosome]] | *Glycogen storage disease type 3 is caused by the deficiency of the glycogen debranching (GDE) enzyme. [[AGL]] [[gene mutation]] responsible for the glycogen debranching (GDE) enzyme deficiency is located on [[chromosome]] 1p21. | ||
==References== | ==References== | ||
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{{WH}} | {{WH}} | ||
{{WS}} | {{WS}} | ||
Revision as of 16:55, 4 December 2017
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Editor-In-Chief: C. Michael Gibson, M.S., M.D. [1]; Associate Editor(s)-in-Chief: Anmol Pitliya, M.B.B.S. M.D.[2]
Overview
Glycogen storage disease type 3 is an autosomal recessive disorder. Glycogen storage disease type 3 is caused by the deficiency of the glycogen debranching (GDE) enzyme. AGL gene mutation responsible for the glycogen debranching (GDE) enzyme deficiency is located on chromosome 1p21.
Causes
- Glycogen storage disease type 3 is an autosomal recessive disorder.
- Glycogen storage disease type 3 is caused by the deficiency of the glycogen debranching (GDE) enzyme. AGL gene mutation responsible for the glycogen debranching (GDE) enzyme deficiency is located on chromosome 1p21.