Volume : IX, Issue : II, February - 2020
AN ENIGMA GORLIN GOLTZ SYNDROME: A RARE CASE REPORT
Dr. Manpreet Singh, Dr. Ankit Kumar, Dr. Pranshu Chauhan, Dr. Sourav Kumar, Dr. Musaab Khan, Dr. Reshu Rastogi
Abstract :
The Gorlin–Goltz syndrome (GGS) (the nevoid basal cell carcinoma syndrome—NBCCS) is a rare autosomal dominant syndrome caused due to mutations in the PTCH (patched) gene found on chromosome arm 9q. The syndrome, characterized by increased predisposition to develop basal cell carcinoma and associated multiorgan anomalies, has a high level of penetrance and variable expressiveness. This case report is of 29 years old male with complaint of pus discharge from upper and lower posterior teeth region since 5 months. On the basis of clinical and radiographic findings provisional diagnosis was made of gorlin –goltz syndrome and was planned for surgical intervention .But the patient deferred the treatment due to financial crisis .patient is recalled after 6 months for follow up.
Keywords :
Article:
Download PDF
DOI : 10.36106/ijsr
Cite This Article:
AN ENIGMA GORLIN GOLTZ SYNDROME: A RARE CASE REPORT, Dr. Manpreet Singh, Dr. Ankit Kumar, Dr. Pranshu Chauhan, Dr.Sourav Kumar, Dr. Musaab Khan, Dr. Reshu Rastogi INTERNATIONAL JOURNAL OF SCIENTIFIC RESEARCH : Volume-9 | Issue-2 | February-2020
Number of Downloads : 405
AN ENIGMA GORLIN GOLTZ SYNDROME: A RARE CASE REPORT, Dr. Manpreet Singh, Dr. Ankit Kumar, Dr. Pranshu Chauhan, Dr.Sourav Kumar, Dr. Musaab Khan, Dr. Reshu Rastogi INTERNATIONAL JOURNAL OF SCIENTIFIC RESEARCH : Volume-9 | Issue-2 | February-2020
Our Other Journals...
-
Indian Journal of
Applied Research Visit Website -
PARIPEX Indian Journal
of Research Visit Website -
Global Journal for
Research Analysis Visit Website