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

• Κύριοι συγγραφείς: Shyam Verma (Συγγραφέας), Sandra M Pasternack (Συγγραφέας), Arno Rutten (Συγγραφέας), Thomas Ruzicka (Συγγραφέας), Regina C Betz (Συγγραφέας), Sandra Hanneken (Συγγραφέας)
• Μορφή: Βιβλίο
• Έκδοση: Wolters Kluwer Medknow Publications, 2014-01-01T00:00:00Z.
• Θέματα: article
• Διαθέσιμο Online: 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...