The first report of krt5 mutation underlying acantholytic dowling-degos disease with mottled hypopigmentation in an Indian family

• Glavni autori: Shyam Verma (Autor), Sandra M Pasternack (Autor), Arno Rutten (Autor), Thomas Ruzicka (Autor), Regina C Betz (Autor), Sandra Hanneken (Autor)
• Format: Knjiga
• Izdano: Wolters Kluwer Medknow Publications, 2014-01-01T00:00:00Z.
• Teme: article
• Online pristup: Connect to this object online.

Galli Galli disease (GGD) is the name given to a rare form of acantholytic Dowling-Degos disease. (DDD), the latter itself being a rare condition. We believe we are describing for the first time in Indian dermatologic literature a case of GGD in a family where 25 persons have DDD and have been able...