Tuesday, 22 October 2013

Inherited metabolic diseases when genetic program fails

It is estimated that one in 1,500 people are born with some of the more than 700 inherited metabolic diseases - Metabolism is a system of living that is responsible for turning food you eat into simpler elements or basic units for reuse, to perform the functions necessary for the body.

 Thanks to the metabolism of proteins, carbohydrates, fats and other substances that are taken as food such units become smaller click the next page
However, the metabolism may fail from birth: one in 1,500 people are born with an altered gene and suffer from any of the over 700 types of inherited metabolic diseases known to date. This article describes how the different symptoms of inherited metabolic disease are and what treatments are available.

What are inherited metabolic diseases?
In the process of metabolism involved enzymes that act as catalysts, i.e. allow different reactions taking place in the body to ingested substances become simpler ones. In turn, these substances called metabolites may be used for the body to synthesize again more complex substances when necessary click the next page

All inherited metabolic diseases characterized by a malfunction of normal metabolism. Source is genetic and is caused by an alteration of DNA (the genetic information of individuals) which leads to the modification of a protein. This change prevents some other substances have become so successively, resulting in a buildup of the substance has not been processed and therefore, the metabolism does not work conveniently.

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