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PNDDB - Pediatric Neurotransmitter Diseases


PNDDB - PTPS deficiency


OMIM 261640


Locus: 11q22.3-23.3
Gene: PTS

Enzyme: 6-Pyruvoyl-tetrahydropterin synthase (EC 4.2.3.12)

Reaction: Dihydroneopterin triphosphate >> 6-Pyruvuoyl-tetrahydropterin + PPP

DD: Mild (peripheral) to severe forms

Diagnosis: Blood, Urine, CSF, DNA
Blood: Phe (high), Neo (high), Bio (low)
Urine: Neo (high), Bio (low)
CSF: Neo (high), 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