Myoadenylate Deaminase Deficiency natural cures

Myoadenylate Deaminase Deficiency Definition

Myoadenylate Deaminase Deficiency or MADD is classified as a metabolic disorder with a recessive genetic cause. This condition affects about 1-2% of the Eastern descent populations which makes it not particularly a rare disease. MADD is somewhat rarer in the Oriental populations. Myoadenylate Deaminase which is also referred to as AMP deaminase is an enzyme responsible in converting adenosine monophosphate or AMP into inosine monophosphate or IMP. This process frees ammonia molecule. This is a portion of metabolic process responsible in converting sugar, fat and protein to cellular energy. A cell usually converts sugar, fat and protein to adenosine triphosphate (ATP) through the mitochondria to utilize energy. Processes within the cell, the muscles in particular then convert ATP to adenosine diphosphate or ADP which frees the energy to perform work. Failure to deaminate AMP molecules covers three major effects which are: 1. The cell and body loses considerable amounts of AMP 2. Ammonia is not freed or released in the event that the cell performs work 3. Maintenance of IMP levels within the cell is impaired

Myoadenylate Deaminase Deficiency Treatment

Sometime, relief from the symptoms associated with MADD can be achieved by oral administration of ribose with a dosage of approximately 10g/100 lbs or 0.2 g/kg body weight per day.

Myoadenylate Deaminase Deficiency Symptoms and Signs

Symptoms associated with this metabolic order include severe fatigue and muscular pains. Absence of ammonia may result in reduction of fumarate amounts available to the citric acid cycle leading to lower levels of nitric oxide, a vasodilator in the body. As a result, reduction in the blood flow and oxygen intake is observed when doing rigorous exercises. Reduction in IMP may result in reduction of lactic acid produced by muscles.

Myoadenylate Deaminase Deficiency Causes

MADD is as a recessive genetic metabolic disorder.


Myoadenylate Deaminase Deficiency by state

Myoadenylate Deaminase Deficiency in Alabama
Myoadenylate Deaminase Deficiency in Alaska
Myoadenylate Deaminase Deficiency in Arizona
Myoadenylate Deaminase Deficiency in Arkansas
Myoadenylate Deaminase Deficiency in Armed Forces
Myoadenylate Deaminase Deficiency in California
Myoadenylate Deaminase Deficiency in Colorado
Myoadenylate Deaminase Deficiency in Connecticut
Myoadenylate Deaminase Deficiency in Delaware
Myoadenylate Deaminase Deficiency in District of Columbia
Myoadenylate Deaminase Deficiency in Florida
Myoadenylate Deaminase Deficiency in Georgia
Myoadenylate Deaminase Deficiency in Hawaii
Myoadenylate Deaminase Deficiency in Idaho
Myoadenylate Deaminase Deficiency in Illinois
Myoadenylate Deaminase Deficiency in Indiana
Myoadenylate Deaminase Deficiency in Iowa
Myoadenylate Deaminase Deficiency in Kansas
Myoadenylate Deaminase Deficiency in Kentucky
Myoadenylate Deaminase Deficiency in Louisiana
Myoadenylate Deaminase Deficiency in Maine
Myoadenylate Deaminase Deficiency in Maryland
Myoadenylate Deaminase Deficiency in Massachusetts
Myoadenylate Deaminase Deficiency in Michigan
Myoadenylate Deaminase Deficiency in Minnesota
Myoadenylate Deaminase Deficiency in Mississippi
Myoadenylate Deaminase Deficiency in Missouri
Myoadenylate Deaminase Deficiency in Montana
Myoadenylate Deaminase Deficiency in Nebraska
Myoadenylate Deaminase Deficiency in Nevada
Myoadenylate Deaminase Deficiency in New Hampshire
Myoadenylate Deaminase Deficiency in New Jersey
Myoadenylate Deaminase Deficiency in New Mexico
Myoadenylate Deaminase Deficiency in New York
Myoadenylate Deaminase Deficiency in North Carolina
Myoadenylate Deaminase Deficiency in North Dakota
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