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Follow-up of a child with pyruvate dehydrogenase deficiency on a less restrictive ketogenic diet.
El-Gharbawy, Areeg H; Boney, Anne; Young, Sarah P; Kishnani, Priya S.
Afiliación
  • El-Gharbawy AH; Division of Medical Genetics, Department of Pediatrics, Duke University Medical Center, 595 La Salle Street, Durham, NC 27710, USA. areeg.el-gharbawy@duke.edu
Mol Genet Metab ; 102(2): 214-5, 2011 Feb.
Article en En | MEDLINE | ID: mdl-21130013
ABSTRACT
A male child with X-linked pyruvate dehydrogenase deficiency presented with severe neonatal lactic acidosis. Poor compliance following initiation of the ketogenic diet justified modification to a less restrictive form which improved compliance. One year after starting the modified diet, he remained clinically stable, showing developmental progress.
Asunto(s)

Texto completo: 1 Base de datos: MEDLINE Asunto principal: Enfermedad por Deficiencia del Complejo Piruvato Deshidrogenasa / Dieta Cetogénica Tipo de estudio: Observational_studies / Prognostic_studies Idioma: En Revista: Mol Genet Metab Asunto de la revista: BIOLOGIA MOLECULAR / BIOQUIMICA / METABOLISMO Año: 2011 Tipo del documento: Article

Texto completo: 1 Base de datos: MEDLINE Asunto principal: Enfermedad por Deficiencia del Complejo Piruvato Deshidrogenasa / Dieta Cetogénica Tipo de estudio: Observational_studies / Prognostic_studies Idioma: En Revista: Mol Genet Metab Asunto de la revista: BIOLOGIA MOLECULAR / BIOQUIMICA / METABOLISMO Año: 2011 Tipo del documento: Article