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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Main Authors: Manal Souali (Author), Asmaa Sakhi (Author), Ahmed Aziz Bousfiha (Author), Kenza Bouayed (Author)
Format: Book
Published: SAGE Publishing, 2023-10-01T00:00:00Z.
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3rd Floor Main Library

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Call Number: A1234.567
Copy 1 Available