Urea cycle disorders: clinical, biochemical and genetic findings in agentinean patients

Urea cycle disorders (UCD) encompass several enzyme deficiencies with a wide clinical spectrum from asymptomatic to severe, mostly with cerebral damage. Objective: to communicate the autochthonous experience in the recognition of UCD. The diagnosis protocol included phenotype compatibility, metabol...

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Autores principales: Laróvere, Laura, Silvera Ruiz, Silene, Arranz, José, Angaroni, Celia, Guelbert, Norberto, Antonozzi, Sandra, Bezard, Miriam, Dodelson de kremer, Raquel
Formato: conferenceObject
Lenguaje:Inglés
Publicado: 2022
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Acceso en línea:http://hdl.handle.net/11086/28160
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