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Ocular Manifestations of Granulomatosis with Polyangiitis: A Review of the Literature

Granulomatosis with polyangiitis (GPA) is a rare systemic autoimmune disease of unknown etiology that is characterized by granulomatous inflammation, tissue necrosis, and vasculitis in small- and medium-sized vessels. Ocular and orbital manifestations are common in almost half of patients with GPA,...

पूर्ण विवरण

में बचाया:
ग्रंथसूची विवरण
में प्रकाशित:Ophthalmol Ther
मुख्य लेखकों: Sfiniadaki, Evdokia, Tsiara, Ioanna, Theodossiadis, Panagiotis, Chatziralli, Irini
स्वरूप: Artigo
भाषा:Inglês
प्रकाशित: Springer Healthcare 2019
विषय:
ऑनलाइन पहुंच:https://ncbi.nlm.nih.gov/pmc/articles/PMC6513923/
https://ncbi.nlm.nih.gov/pubmed/30875067
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1007/s40123-019-0176-8
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