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PNDDB - arGTPCH deficiency
OMIM 233910
Enzyme: GTP cyclohydrolase I (EC 3.5.4.16)
Reaction: GTP >> Dihydroneopterin triphosphate + Formiate
DD: adGTPCH deficiency (Segawa disease)
Diagnosis: Blood, Urine, CSF, DNA Blood: Phe (high), Neo (low), Bio (low) Urine: Neo (low), Bio (low) CSF: Neo (low), Bio (low), 5HIAA (low), HVA (low) DNA: see PNDDB
Clinical signs & symptoms: Progressive dystonia Truncal hypotonia Hypertonia of extremities Hypersalivation Choreoathetoosis Seizures Mental retardation
Treatment: L-Dopa/Carbidopa (10 or 25%) <15 mg/kg/d - 3-6 doses/day 5-OH-Trp <9 mg/kg/d - 3-6 doses/day Tetrahydrobiopterin 5-10 mg/kg/d - 2 doses/day
Alternative treatment: Deprenyl 0.1-0.3 mg/kg/d - 3-4 doses/day Entacapone <30 mg/kg/d - 1-2 doses