Phenylketonuria variant

Phenylketonuria (PKU) is an inborn error of metabolism that results in decreased metabolism of the amino acid phenylalanine. Untreated, PKU can lead to intellectual disability, seizures, behavioral problems, and mental disorders. [Source: Wikipedia ]

Synonyms
Mild phenylketonuria
Mild PKU
MPKU
Variant phenylketonuria
Variant PKU
OrphaNet reference
Mild phenylketonuria 
May Cause
Basal ganglion calcification
Mild phenylketonuria
Mild PKU
MPKU
Variant phenylketonuria
Variant PKU