Nakajo-Nishimura Syndrome: The First African Case

Nakajo-Nishimura syndrome is a hereditary autoinflammatory disorder caused by an autosomal recessive homozygous mutation of the PSMB8 gene, which encodes the immunoproteasome subunit beta 5i. The clinical manifestations of NNS are mainly pernio-like skin rashes, nodular erythema, lipodystrophy, club...

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Detalles Bibliográficos
Autores principales: Ghodbane, Nacif Eddine, Mecibah, Ali, Merzougui, Zohra, Zerguine, Halima, Akakba, Zineb, Slimani, Samy
Formato: Online Artículo Texto
Lenguaje:English
Publicado: The Mediterranean Journal of Rheumatology (MJR) 2023
Materias:
Case Report
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10466351/
https://www.ncbi.nlm.nih.gov/pubmed/37654638
http://dx.doi.org/10.31138/mjr.34.2.262

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10466351/
https://www.ncbi.nlm.nih.gov/pubmed/37654638
http://dx.doi.org/10.31138/mjr.34.2.262

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