Vogt–Koyanagi–Harada (VKH) syndrome: A new perspective for healthcare professionals

Vogt–Koyanagi–Harada syndrome (VKH syndrome) is a rare granulomatous inflammatory disease that affects the melanin pigment producing melanocytes and mainly affects the pigmented structures such as eyes, ear, skin, meninges, and hair. VKT is an autoimmune disorder, which is mainly a T CD4+ Th1 lympho...

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Autors principals:	Yojana B Patil, Ruchira Garg, Jagadish Prasad Rajguru, Manjunath Sirsalmath, Varsha A Bevinakatti, Manish Kumar, Sonika Sharma
Format:	Artigo
Idioma:	Inglês
Publicat:	Wolters Kluwer Medknow Publications 2020-01-01
Col·lecció:	Journal of Family Medicine and Primary Care
Matèries:	melanin syndrome vkh
Accés en línia:	http://www.jfmpc.com/article.asp?issn=2249-4863;year=2020;volume=9;issue=1;spage=31;epage=35;aulast=Patil
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