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Urea cycle defects: management and outcome
M C Nassogne1, B Héron, G Touati
1Paediatric Neurology Unit, Department of Paediatrics, Saint-Luc Hospital Brussels, Belgium. marie-cecile.nassogne@nepe.ucl.ac.be
Abstract:
This paper reviews the clinical presentation of 217 patients with urea cycle defects, including 121 patients with neonatal-onset forms and 96 patients with late-onset forms. Long-term outcome of these patients is also reported with the severity of the neonatal forms of these disorders, mostly for ornithine carbamoyltransferase-deficient males. Patients with late-onset forms may present at any age and carry a 28% mortality rate and a subsequent risk of subsequent disabilities.
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