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Weekly oral alendronate in mevalonate kinase deficiency
BACKGROUND: Mevalonate kinase deficiency (MKD) is caused by mutations in the MVK gene, encoding the second enzyme of mevalonate pathway, which results in subsequent shortage of downstream compounds, and starts in childhood with febrile attacks, skin, joint, and gastrointestinal symptoms, sometimes i...
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| Main Authors: | , , , , , , , |
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| Formato: | Artigo |
| Idioma: | Inglês |
| Publicado em: |
BioMed Central
2013
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| Assuntos: | |
| Acesso em linha: | https://ncbi.nlm.nih.gov/pmc/articles/PMC3880037/ https://ncbi.nlm.nih.gov/pubmed/24360083 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1186/1750-1172-8-196 |
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