Phenylketonuria and juvenile idiopathic arthritis: a case report

BACKGROUND: Phenylketonuria (PKU) is a genetic metabolic disorder in which patients have no ability to convert phenylalanine to tyrosine. Several autoimmune diseases have been reported to combine with PKU, co-existent of PKU and Juvenile Idiopathic Arthritis (JIA) has not been presented. CASE PRESEN...

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Detalles Bibliográficos
Autores principales: Zhu, Ting Ting, Wu, Jin, Wang, Li Yuan, Sun, Xiao Mei
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2021
Materias:
Case Report
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7962320/
https://www.ncbi.nlm.nih.gov/pubmed/33722205
http://dx.doi.org/10.1186/s12887-021-02602-6

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7962320/
https://www.ncbi.nlm.nih.gov/pubmed/33722205
http://dx.doi.org/10.1186/s12887-021-02602-6

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