[Scleroderma-like changes in phenylketonuria].
D006801:Humans; D007223:Infant; D008297:Male; D010661:Phenylketonurias / Q000150:complications*; D012595:Scleroderma, Systemic / Q000209:etiology*; D014364:Tryptophan / Q000378:metabolism*
D014364:Tryptophan
Twardzinopodobne zmiany w fenyloketonurii.