Co-existence of Phenylketonuria and Fabry disease on a 3 year-old boy: case report

BACKGROUND: The co-existence of two genetically distinct metabolic disorders in the same patient has rarely been reported. Phenylketonuria (PKU) is an inborn error of the metabolism resulting from a phenylalanine hydroxylase deficiency. Fabry disease (FD) is an X-linked lysosomal storage disorder du...

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Detalles Bibliográficos
Autores principales: Concolino, Daniela, Rapsomaniki, Maria, Disabella, Eliana, Sestito, Simona, Pascale, Maria G, Moricca, Maria T, Bonapace, Giuseppe, Arbustini, Elisea, Strisciuglio, Pietro
Formato: Texto
Lenguaje:English
Publicado: BioMed Central 2010
Materias:
Case report
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2885380/
https://www.ncbi.nlm.nih.gov/pubmed/20478016
http://dx.doi.org/10.1186/1471-2431-10-32

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2885380/
https://www.ncbi.nlm.nih.gov/pubmed/20478016
http://dx.doi.org/10.1186/1471-2431-10-32

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