Defects in Amino Acid Metabolism
Phenylketonuria
Type I Tyrosinemia -Tyrosinosis
Type II Tyrosinnemia -Richner-Hanhart Syndrome
Type III Tyrosinemia
Alcaptonuria
Homocystinuria
Histidinemia
Maple Syrup Urine Disease, MSUD
Methylmalonic Aciduria
Non-ketonic Hyperglycinemia Type I (NKHI)
Hyperlysinemia
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Michael W. King, Ph.D / IU School of Medicine / miking at iupui.edu