What is an Acyl-CoA Dehydrogenase, Medium Chain, Deficiency?

April 21 22:14 2019 Print This Article

It is defined as a condition in which there is a problem in the oxidation of fatty acids which is in connection with the errors of metabolism which are present when the person is borne. There is a problem in the complex of enzyme and is referred as the medium chain acyl dehydrogenase referred as the MCAD. It oxidizes the medium chain fatty acids. It can even lead to the sudden death of infant.

What is the etiology of Acyl-CoA Dehydrogenase, Medium Chain, Deficiency?

It is due to the problem in the complex of enzyme and is referred as the medium chain acyl dehydrogenase referred as the MCAD. It oxidizes the medium chain fatty acids. It can even lead to the sudden death of infant.

What is the treatment of Acyl-CoA Dehydrogenase, Medium Chain, Deficiency?

There is no definite treatment for this disorder. But one can prevent the adverse effects. One must never fast for 10 to 12 hours a day. The patient may take intra venous glucose if there is a loss of appetite or a severe vomiting. It is done so that the fat is not used.

What are the preventive measures of Acyl-CoA Dehydrogenase, Medium Chain, Deficiency?

The patient must depend on low fat diet. He must take carnitine daily and it decreases the toxic accumulation of fatty acids as they are excreted in the urine. The increase in intake of alcohol or long fasting makes the condition worsen further.