3-hydroxy-3-methylglutaric aciduria (HMG)

Overview

What is 3-Hydroxy-3-Methylglutaric Aciduria (HMG) disease?

3-hydroxy-3-methylgutaric aciduria or HMG lyase deficiency is a metabolic disorder that causes the body to not be able to break down a protein building block (amino acid) that is referred to as leucine. This syndrome also affects the body from making “ketones” which the body uses for energy during fasting, illness or physiological stress.

SOURCE: Emory University - Department of Human Genetics in collaboration with ThinkGenetic • https://www.thinkgenetic.com/diseases/3-hydroxy-3-methylglutaric-aciduria-hmg/overview/17004 • DATE UPDATED: 2016-07-08

References

This content comes from a hidden element on this page.

The inline option preserves bound JavaScript events and changes, and it puts the content back where it came from when it is closed.

Remember Me