First case of hereditary xanthinuria in a Moroccan family
The xanthinuria is a rare hereditary autosomal recessive disease. It is related to xanthine oxidase deficiency also known as xanthine dehydrogenase, an enzyme involved in the metabolism of purine bases. In this work, we describe the first cases of hereditary xanthinuria in a Moroccan family. We repo...
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| Principais autores: | , , , , |
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| Formato: | Artigo |
| Idioma: | Inglês |
| Publicado em: |
PAMJ
2019-12-01
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| coleção: | PAMJ Clinical Medicine |
| Assuntos: | |
| Acesso em linha: |
https://www.clinical-medicine.panafrican-med-journal.com/content/article/1/55/pdf/55.pdf
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