Glycogen storage disease type 1B natural cures

Glycogen storage disease type 1B Definition

Glycogen storage disease type 1B, also known as von Gierke's disease, is the most common form among the glycogen storage diseases. An enzyme glucose-6-phosphate deficiency is the cause of this, affecting the liver's ability in producing free glucose from gluconeogenesis and glycogen. This in turn, may result in hypoglycemia.

Glycogen storage disease type 1B Diagnosis

If a patient exhibits the symptoms mentioned above, diagnosis of glycogen storage type 1B is suspected. If he shows additional symptoms such as hyperuricemia, enlarged kidneys, lactic acidosis, and hypertriglyceridemia, then the diagnosis for this disease strengthens. Monitored fasting is also another procedure in the diagnosis for GSD type 1B. If he is positive for the disease, he will develop hypoglycemia within 6 hours. To confirm this, a liver biopsy will be conducted accompanied by an electron microscopy.

Glycogen storage disease type 1B Symptoms and Signs

The symptoms usually present themselves by 2 years of age. These include hepatomegaly, seizures, other appearances of severe fasting hypoglycemia, vomiting sometimes accompanied by minor illness and hypoglycemia, respiratory difficulties, and hyperventilation. ................................................................................................................................................ Glycogen storage disease type 1B is autosomal recessive in nature, although the carriers, or the patient's parents, tend to be asymptomatic. Its incidence in the United States is 1 in 100,000 or 200,000.

Glycogen storage disease type 1B Causes

In order to prevent hypoglycemia, treatment must include regular feeding of glucose and start products. The dietary carbohydrate must equivalent the body's glucose production rate in 24 hours. Ideally the diet should be composed of 10-15% protein, 20-25% fat, and 65-70% carbohydrate. One-thirds of the carbohydrates should be supplied at nighttime so that patients do not go over 4 hours without any carbohydrates. Other forms of sugars, such as fructose and galactose, must be avoided.


Glycogen storage disease type 1B by state

Glycogen storage disease type 1B in Alabama
Glycogen storage disease type 1B in Alaska
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Glycogen storage disease type 1B in Arkansas
Glycogen storage disease type 1B in Armed Forces
Glycogen storage disease type 1B in California
Glycogen storage disease type 1B in Colorado
Glycogen storage disease type 1B in Connecticut
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Glycogen storage disease type 1B in District of Columbia
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Glycogen storage disease type 1B in Hawaii
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Glycogen storage disease type 1B in Maryland
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Glycogen storage disease type 1B in Mississippi
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Glycogen storage disease type 1B in Nebraska
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Glycogen storage disease type 1B in New Hampshire
Glycogen storage disease type 1B in New Jersey
Glycogen storage disease type 1B in New Mexico
Glycogen storage disease type 1B in New York
Glycogen storage disease type 1B in North Carolina
Glycogen storage disease type 1B in North Dakota
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