Gorlin syndrome: A case report

Autor: Abbas Darjani, Hojat Eftekhari, Nahid Nickhah
Jazyk: English<br />Spanish; Castilian<br />French<br />Polish
Rok vydání: 2016
Předmět:
Zdroj: Nasza Dermatologia Online, Vol 7, Iss 1, Pp 72-74 (2016)
Druh dokumentu: article
ISSN: 2081-9390
DOI: 10.7241/ourd.20161.18
Popis: Gorlin syndrome is a rare autosomal dominant disorder which characterize by multi-organ abnormities such as odontogenic keratocysts in the jaw, skeletal abnormities and multiple basal cell carcinoma etc. We report a case of this syndrome in a young man with palmar pits, multiple facial BCC, clacifications of the falx cerebri and bifid rib.
Databáze: Directory of Open Access Journals