GORLIN'S SYNDROME: CASE REPORT AND MANAGEMENT PROTOCOL

Rosti R. O., Aktas I., Kayserili H., Yalcin S.

BALKAN JOURNAL OF MEDICAL GENETICS, cilt.12, sa.1, ss.61-65, 2009 (SCI-Expanded) identifier identifier

  • Yayın Türü: Makale / Tam Makale
  • Cilt numarası: 12 Sayı: 1
  • Basım Tarihi: 2009
  • Doi Numarası: 10.2478/v10034-009-0002-z
  • Dergi Adı: BALKAN JOURNAL OF MEDICAL GENETICS
  • Derginin Tarandığı İndeksler: Science Citation Index Expanded (SCI-EXPANDED), Scopus
  • Sayfa Sayıları: ss.61-65
  • İstanbul Üniversitesi Adresli: Evet

Özet

Gorlin's syndrome (GS) is a rare autosomal, dominant syndrome, characterized by multiple basal cell carcinomas, odontogenic keratocysts, a characteristic facial appearance, skeletal anomalies and malignancies of various organs throughout the body. We describe a 14-year-old girl with GS and propose a management protocol.