Add more rows to at least have 4 examples thanks Search for

Add more rows to at least have 4 examples. thanks

Search for inborn errors of metabolism and/or metabolic disorders. Describe what the error/defect is of at least one type using the listed sites for reference.

Solution

Certain aminoacid of proteins such as leucine, isoleucine, and valine. cannot be broken down and so they build up in urine..Urine of affected people smells like maple syrup.

Hereditary fructose intolerance

Error/Disorder	Disease Name/Number	Phenotype and description	Source /Citation
Inability in babies to break down phenylalanine aminoacid due to lack of enzyme phenylalanine hydroxylase.	Phenylketonuria	Light colored hair, skin ,eyes,small head size, skin rashes.	https://medlineplus.gov/ency/article/001166.htm
Certain aminoacid of proteins such as leucine, isoleucine, and valine. cannot be broken down and so they build up in urine..Urine of affected people smells like maple syrup.	Maple syrup urine disease	People have feeding problems,body shakes uncontrollably,people often feel fatigue,may go to coma.	https://medlineplus.gov/ency/article/000373.htm
Body fails to metabolise galactose sugar due to deficiency of either galactose kinase,galactose-6-phosphate epimeraseor galactose-1 phosphate uridyl transferase enzymes.	Galactosemia	Reduced weight, skin turns yellow and eyes become white that is a sign of jaundice.	https://medlineplus.gov/ency/article/000366.htm
Body cannot break down fructose due to deficiency of aldolase B enzyme.	Hereditary fructose intolerance	Skin turns yellow and eyes become white that is a sign of jaundice	https://medlineplus.gov/ency/article/000359.htm