Literature DB >> 21958180

Vogt-Koyanagi-Harada syndrome: review of clinical features.

David Pan1, Tatsuo Hirose.   

Abstract

Vogt-Koyanagi-Harada syndrome is a bilateral, chronic, diffuse granulomatous panuveitis associated with poliosis, vitiligo, and central nervous system and auditory signs. Increasing reports have been published to describe the clinical features of Vogt-Koyanagi-Harada syndrome. These manifestations are variable. This article presents a review of the clinical features.

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Year:  2011        PMID: 21958180     DOI: 10.3109/08820538.2011.588654

Source DB:  PubMed          Journal:  Semin Ophthalmol        ISSN: 0882-0538            Impact factor:   1.975


  4 in total

Review 1.  Autoimmune uveitis: clinical, pathogenetic, and therapeutic features.

Authors:  Marcella Prete; Rosanna Dammacco; Maria Celeste Fatone; Vito Racanelli
Journal:  Clin Exp Med       Date:  2015-03-28       Impact factor: 3.984

2.  Acute lupus choroidopathy: multimodal imaging and differential diagnosis from central serous chorioretinopathy.

Authors:  Murat Hasanreisoglu; Gokcen D Gulpinar Ikiz; Hamit Kucuk; Ozkan Varan; Sengul Ozdek
Journal:  Int Ophthalmol       Date:  2017-01-03       Impact factor: 2.031

3.  Secondary angle closure glaucoma by lupus choroidopathy as an initial presentation of systemic lupus erythematosus: a case report.

Authors:  Young Soo Han; Chan min Yang; Sang-Hoon Lee; Jae Ho Shin; Sang Woong Moon; Ja Heon Kang
Journal:  BMC Ophthalmol       Date:  2015-10-29       Impact factor: 2.209

Review 4.  Autoimmunity in visual loss.

Authors:  Axel Petzold; Sui Wong; Gordon T Plant
Journal:  Handb Clin Neurol       Date:  2016
  4 in total

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