Final answer:
Medium Chain Fatty Acyl CoA Dehydrogenase Deficiency (MCADD) is a genetic disorder that affects the metabolism of fatty acids.
Step-by-step explanation:
Medium Chain Fatty Acyl CoA Dehydrogenase Deficiency (MCADD) is a genetic disorder that affects the metabolism of fatty acids.
It is caused by a deficiency of the enzyme medium chain acyl-CoA dehydrogenase, which is responsible for breaking down medium chain fatty acids.
This deficiency can lead to a buildup of fatty acids in the body, which can cause a variety of symptoms such as low blood sugar, lethargy, and vomiting. MCADD is typically diagnosed at birth through newborn screening and can be managed through dietary modifications and close monitoring of blood sugar levels.