<abstract xml:lang="en" xmlns="http://www.w3.org/1999/xhtml"><p>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.</p></abstract>

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.

Gorlin's Syndrome: Case Report and Management Protocol

Department of Medical Genetics, Istanbul Medical Faculty, Istanbul University, Istanbul, Turkey

Department of Oral Surgery, Faculty of Dentistry, Istanbul University, Istanbul, Turkey

Balkan Journal of Medical Genetics

{"article-title":"Gorlin's Syndrome: Case Report and Management Protocol"}

Gorlin's syndrome (GS) is a rare autosomal, dominant syndrome, characterized by multiple basal cell carcinomas, odontogenic keratocysts, a characteristic...

Gorlin's Syndrome: Case Report and Management Protocol

Pubblicato online: 09 ott 2009

Pagine: 61 - 64

DOI: https://doi.org/10.2478/v10034-009-0002-z

Parole chiave
Basal cell carcinomas, Gorlin's syndrome (GS), Odontogenic keratocysts, Palmar/plantar pits, PTCH1

This content is open access.

Gorlin's Syndrome: Case Report and Management Protocol

Pubblicato online: 09 ott 2009

Pagine: 61 - 64

DOI: https://doi.org/10.2478/v10034-009-0002-z

Parole chiaveBasal cell carcinomas, Gorlin's syndrome (GS), Odontogenic keratocysts, Palmar/plantar pits, PTCH1

This content is open access.

Parole chiave
Basal cell carcinomas, Gorlin's syndrome (GS), Odontogenic keratocysts, Palmar/plantar pits, PTCH1