Cargando…
A rare case of NXP-2 positive dermatomyositis
Dermatomyositis is an idiopathic inflammatory myopathy with variable cutaneous manifestations. Several autoantibodies each with distinct clinical phenotypes are associated with the disease. Here we present the case of a 36-year-old Laotian woman with hypothyroidism who presented with severe proximal...
Autores principales: | Khan, Nariman, Kazmi, Zehra Hasan, Alkhateb, Rahaf |
---|---|
Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
UMF “Gr. T. Popa” Iasi Publishing House
2021
|
Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8565706/ https://www.ncbi.nlm.nih.gov/pubmed/34754931 http://dx.doi.org/10.22551/2020.29.0704.10176 |
Ejemplares similares
-
NXP-2 Positive Dermatomyositis: A Unique Clinical Presentation
por: Butt, Zeeshan, et al.
Publicado: (2017) -
Triple whammy: a rare case of epithelioid hemangioendothelioma with synchronous angiomyomatous hamartoma complicated by Actinomyces meyeri
por: Khan, Nariman, et al.
Publicado: (2021) -
Corrigendum to “NXP-2 Positive Dermatomyositis: A Unique Clinical Presentation”
por: Butt, Zeeshan, et al.
Publicado: (2018) -
A Rare Case of Anti-HMGCR and Anti-SRP-Positive Immune-Mediated Necrotizing Myopathy
por: Khan, Nariman, et al.
Publicado: (2022) -
A Case of Dermatomyositis Coexisting with Both Anti-Mi-2 and Anti-NXP-2 Antibodies
por: Ito, Mitsuru, et al.
Publicado: (2020)