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...
| Published in: | Global Pediatric Health |
|---|---|
| Main Authors: | , , , |
| Format: | Article |
| Language: | English |
| Published: |
SAGE Publishing
2023-10-01
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| Online Access: | https://doi.org/10.1177/2333794X231207351 |