Efficacy of Anakinra Treatment in two Moroccan Patients With Mevalonate Kinase Deficiency

Mevalonate kinase deficiency (MKD) is a rare hereditary autoinflammatory disease, with a widely variable clinical spectrum. It is characterized by febrile recurrent episodes and systemic inflammation. Data on therapeutic options for MKD are still limited and remain unknown in our country. We report...

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Detalles Bibliográficos
Autores principales: Souali, Manal, Sakhi, Asmaa, Bousfiha, Ahmed Aziz, Bouayed, Kenza
Formato: Online Artículo Texto
Lenguaje:English
Publicado: SAGE Publications 2023
Materias:
Case Report
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10605664/
https://www.ncbi.nlm.nih.gov/pubmed/37901181
http://dx.doi.org/10.1177/2333794X231207351

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10605664/
https://www.ncbi.nlm.nih.gov/pubmed/37901181
http://dx.doi.org/10.1177/2333794X231207351

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