The list of signs and symptoms mentioned in various sources for Glycogen storage disease type 2 includes the 28 symptoms listed below:
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Primary clinical features of the liver glycogen storage diseases (Types I, III, IV, VI, and VIII) are hepatomegaly and rapid onset of hypoglycemia and ketosis when food is withheld. Symptoms of the muscle glycogen storage diseases (Types II, V, and VII) include poor muscle tone; Type II may result in death from heart failure. (See Rare forms of glycogen storage disease.)
In addition, Type I may produce these symptoms:
❑ infants: acidosis, hyperlipidemia, GI bleeding, coma
❑ children: low resistance to infection and, without proper treatment, short stature
❑ adolescents: gouty arthritis and nephropathy; chronic tophaceous gout; bleeding (especially epistaxis); small superficial vessels visible in skin due to impaired platelet function; fat deposits in cheeks, buttocks, and subcutaneous tissues; poor muscle tone; enlarged kidneys; xanthomas over extensor surfaces of arms and legs; steatorrhea; multiple, bilateral, yellow lesions in fundi; and osteoporosis, probably secondary to negative calcium balance. Correct treatment of glycogen storage disease should prevent all of these effects.
Source: Professional Guide to Diseases (Eighth Edition), 2005
Primary clinical features of liver glycogen storage disease (types I, III, IV, VI, and VIII) are hepatomegaly and rapid onset of hypoglycemia and acidosis when food is withheld. Symptoms of muscle glycogen storage disease (types II, V, and VII) include poor muscle tone; type II may result in death from heart failure.
In addition, type I may produce the following symptoms:
❑ infants — acidosis, hyperlipidemia, GI bleeding, coma
❑ children — low resistance to infection and, without proper treatment, short stature
❑ adolescents — gouty arthritis and nephropathy; chronic tophaceous gout; bleeding (especially epistaxis); small superficial vessels visible in skin because of impaired platelet function; and fat deposits in cheeks, buttocks, and subcutaneous tissues.
Other symptoms include poor muscle tone; enlarged kidneys; xanthomas over extensor surfaces of the arms and legs; steatorrhea; multiple, bilateral, yellow lesions in fundi; and osteoporosis, probably secondary to a negative calcium balance. Proper treatment of glycogen storage disease should prevent all these effects.
Source: Handbook of Diseases, 2003
When considering symptoms of Glycogen storage disease type 2, it is also important to consider Glycogen storage disease type 2 as a possible cause of other medical conditions. The Disease Database lists the following medical conditions that Glycogen storage disease type 2 may cause:
These general reference articles may be of interest in relation to medical signs and symptoms of disease in general:
Full list of premium articles on symptoms and diagnosis
The symptom information on this page attempts to provide a list of some possible signs and symptoms of Glycogen storage disease type 2. This signs and symptoms information for Glycogen storage disease type 2 has been gathered from various sources, may not be fully accurate, and may not be the full list of Glycogen storage disease type 2 signs or Glycogen storage disease type 2 symptoms. Furthermore, signs and symptoms of Glycogen storage disease type 2 may vary on an individual basis for each patient. Only your doctor can provide adequate diagnosis of any signs or symptoms and whether they are indeed Glycogen storage disease type 2 symptoms.
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