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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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| Pubblicato in: | BMC Pediatr |
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| Autori principali: | , , , |
| Natura: | Artigo |
| Lingua: | Inglês |
| Pubblicazione: |
BioMed Central
2021
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| Soggetti: | |
| Accesso online: | https://ncbi.nlm.nih.gov/pmc/articles/PMC7962320/ https://ncbi.nlm.nih.gov/pubmed/33722205 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1186/s12887-021-02602-6 |
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