Follow-up of a child with pyruvate dehydrogenase deficiency on a less restrictive ketogenic diet.
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.
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