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(E71) Disorders of branched-chain amino-acid metabolism and fatty-acid metabolism
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44 219 in individuals diagnosis disorders of branched-chain amino-acid metabolism and fatty-acid metabolism confirmed
3 231 deaths with diagnosis disorders of branched-chain amino-acid metabolism and fatty-acid metabolism
7% mortality rate associated with the disease disorders of branched-chain amino-acid metabolism and fatty-acid metabolism
Diagnosis disorders of branched-chain amino-acid metabolism and fatty-acid metabolism is diagnosed Men are 10.59% more likely than Women
24 451
Men receive the diagnosis disorders of branched-chain amino-acid metabolism and fatty-acid metabolism
1 825 (7.5 %)Died from this diagnosis.
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19 768
Women receive the diagnosis disorders of branched-chain amino-acid metabolism and fatty-acid metabolism
1 406 (7.1 %)Died from this diagnosis.
Risk Group for the Disease disorders of branched-chain amino-acid metabolism and fatty-acid metabolism - Men and Women aged 0-5
In Men diagnosis is most often set at age 0-39, 45-64
Less common in men the disease occurs at Age 40-44, 65-95+Less common in women the disease occurs at Age 30-95+
In Women diagnosis is most often set at age 0-29
Disease Features disorders of branched-chain amino-acid metabolism and fatty-acid metabolism
Absence or low individual and public risk
Disorders of branched-chain amino-acid metabolism and fatty-acid metabolism - what does this mean
Disorders of branched-chain amino-acid metabolism and fatty-acid metabolism occur when the body is unable to properly break down certain proteins and fats, resulting in the accumulation of toxic metabolites in the body. these disorders are caused by genetic mutations that affect the enzymes responsible for breaking down these molecules, leading to a variety of symptoms such as poor growth, developmental delays, and seizures. treatment typically involves dietary management and supplementation of specific nutrients to help manage symptoms.
What happens during the disease - disorders of branched-chain amino-acid metabolism and fatty-acid metabolism
Disorders of branched-chain amino-acid metabolism and fatty-acid metabolism occur when the enzymes responsible for metabolizing these molecules are mutated or absent, leading to an accumulation of these molecules in the body. this can cause a variety of symptoms, such as poor growth, seizures, and developmental delays. in some cases, the accumulation of these molecules can also lead to the development of fatty liver disease.
Clinical Pattern
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How does a doctor diagnose
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Treatment and Medical Assistance
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14 Days of Hospitalization Required
Average Time for Outpatient Care Not Established
Disorders of branched-chain amino-acid metabolism and fatty-acid metabolism - Prevention
Prevention of disorders of branched-chain amino-acid metabolism and fatty-acid metabolism can be achieved through dietary interventions, such as avoiding processed foods and increasing intake of fresh fruits and vegetables. additionally, regular exercise and adequate sleep can help improve metabolism and reduce the risk of metabolic disorders.