An inherited disorder in which the body cannot process particular protein building blocks (amino acids) which are used for energy especially during periods without food (fasting) or when sick.
2,4-Dienoyl-CoA reductase deficiency (DE RED)
An inherited disorder associated with hypotonia and respiratory acidosis in infancy. This condition may be associated with the DECR1 gene and likely has an autosomal recessive pattern of inheritance.
Glutaric acidemia type I (GA-1)
An inherited disorder in which the body cannot process particular protein building blocks (amino acids) called lysine, hydroxylysine, and tryptophan.
