What is the prognosis for an individual with Glycogen Storage Disease Type Ia? With careful monitoring of diet and blood sugar levels, individuals with GSDIa typically have normal growth and live into adulthood. Without close monitoring of the diet, extremely low blood sugar levels can be fatal.

What is the life expectancy of someone with glycogen storage disease?

What is the prognosis for an individual with Glycogen Storage Disease Type Ia? With careful monitoring of diet and blood sugar levels, individuals with GSDIa typically have normal growth and live into adulthood. Without close monitoring of the diet, extremely low blood sugar levels can be fatal.

What is von Gierke’s disease?

Von Gierke disease is a condition in which the body cannot break down glycogen. Glycogen is a form of sugar (glucose) that is stored in the liver and muscles. It is normally broken down into glucose to give you more energy when you need it. Von Gierke disease is also called Type I glycogen storage disease (GSD I).

What causes the symptoms of Cori’s disease?

Glycogen storage disease type III (also known as GSDIII or Cori disease) is an inherited disorder caused by the buildup of a complex sugar called glycogen in the body’s cells. The accumulated glycogen is structurally abnormal and impairs the function of certain organs and tissues, especially the liver and muscles.

What are the symptoms of glycogen storage disease?

What are the symptoms of glycogen storage disease in a child?

  • Not growing fast enough.
  • Not feeling comfortable in hot weather (heat intolerance)
  • Bruising too easily.
  • Low blood sugar (hypoglycemia)
  • An enlarged liver.
  • A swollen belly.
  • Weak muscles (low muscle tone)
  • Muscle pain and cramping during exercise.

Is glycogen storage disease fatal?

Because they affect so many organ systems, GSD Type II (Pompe’s disease) and GSD Type IV (Andersen’s disease) are very hard to treat and can be fatal. Research into enzyme replacement therapy and gene therapy is promising, which may improve the outlook for the future.

What is Gaucher disease?

Gaucher disease is a rare genetic disorder passed down from parents to children (inherited). When you have Gaucher disease, you are missing an enzyme that breaks down fatty substances called lipids. Lipids start to build up in certain organs such as your spleen and liver. This can cause many different symptoms.

What is McArdle’s syndrome?

McArdle disease (GSD 5) is a rare, genetic muscle disorder. It is an inherited disease. It is a type of glycogen storage disease. It results from a lack of a key substance that the muscles need to break down glycogen into sugar (glucose) for energy. The condition causes tiredness and muscle pain during exercise.

Is there a cure for Cori’s disease?

Treatment. There is not currently a cure for for glycogen storage disease type 3 (GSDIII). In some cases, diet therapy is helpful. Strict adherence to a dietary regimen may reduce liver size, prevent hypoglycemia (low blood sugar), help to reduce symptoms, and allow for growth and development.

What organ is malfunctioning in glycogen storage disorder?

Since glycogen is primarily stored in the liver or muscle tissue, glycogen storage diseases usually affect functioning of the liver, the muscles, or both. The glycogen storage diseases that mainly affect the liver are types I, III, IV, and VI.