About Glycogen Storage Disease Type 3

Glycogen Storage Disease Iii, also known as glycogen storage disease type iii, is related to atrial standstill 1 and hypertrophic cardiomyopathy. An important gene associated with Glycogen Storage Disease Iii is AGL (Amylo-Alpha-1, 6-Glucosidase, 4-Alpha-Glucanotransferase), and among its related pathways/superpathways are Metabolism and Disease. The drugs Famotidine and Cetirizine have been mentioned in the context of this disorder. Affiliated tissues include liver, heart and eye, and related phenotypes are short stature and intellectual disability, mild

Major Symptoms of Glycogen Storage Disease Type 3

Glycogen storage disease type 3, also known as Pompe disease, is a rare genetic disorder that affects the body's ability to store and process glycogen, leading to a range of symptoms. Some of the major symptoms of Glycogen storage disease type 3 include:

1. Juvenile onset: This means that the symptoms typically appear in children or adolescents.

2. progressive muscle weakness: This results from the progressive loss of muscle mass and strength due to the disease's effects on the body's ability to store and process glycogen.

3. Facial Fatigue and muscle weakness: Many people with Glycogen storage disease type 3 experience fatigue and muscle weakness, which can make daily activities difficult.

5. Swollen and joint pain: This can result from the disease's effects on the body's connective tissue, which can cause swelling and joint pain.

6. Short stature: This is due to the progressive loss of muscle mass and strength due to the disease's effects on the body's ability to store and process glycogen.

7. Low blood cell counts: As a result of the disease's effects on the body's ability to store and process glycogen, many people with Glycogen storage disease type 3 have low blood cell counts.

8. Inherited from parents: This is an inherited disorder that is passed down from parents to their children through the transmission of a genetic mutation.

Suitable Lifestyle for People with Glycogen Storage Disease Type 3

Glycogen storage disease type 3 is a hereditary liver disease in which the patient's ability to store glycogen in the liver is reduced, leading to liver damage and abnormal function. People suffering from this disease need to pay attention to their diet and lifestyle to reduce the damage of the disease to the body. First of all, patients should avoid overeating and the diet should be based on the principles of low sugar, low fat, high protein, and high fiber. It is recommended to increase the intake of vegetables, fruits, whole grains, high-quality protein, healthy fats and fiber in moderation, while limiting the intake of sugar, alcohol and caffeine. Secondly, patients should maintain good living habits, including regular work and rest, moderate exercise, and reducing stress. Get enough sleep and avoid overwork and fatigue to reduce the burden on your liver. In addition, patients should also pay attention to avoid damage to the liver from infections, drugs, and toxins, undergo regular examinations and treatments, maintain a good attitude, and actively cooperate with treatment to improve treatment effects and quality of life. In short, people suffering from Glycogen storage disease type 3 should pay attention to their diet and lifestyle, maintain good living habits and mentality, and actively cooperate with treatment to reduce the damage of the disease to the body.

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