Gorlin-Goltz syndrome: Case report

Authors

  • Mayank M Mahajan Sumandeep Vidyapeeth University
  • Sagar R Gupta Sumandeep Vidyapeeth University
  • Yash D Shah Sumandeep Vidyapeeth University
  • Honeypalsinh H Maharaul Sumandeep vidyapeeth university
  • Sanjay Vaghani Sumandeep Vidyapeeth University

DOI:

https://doi.org/10.7439/ijbr.v5i10.742

Abstract

Gorlin-Goltz syndrome, also known as basal cell nevus syndrome, is an uncommon, autosomal dominant inherited disorder, which is characterized by numerous basal cell carcinomas, maxillary keratocysts, and musculoskeletal malformations. Occasionally, it is associated with aggressive basal cell carcinomas and internal malignancies. Early diagnosis and treatment are essential, as well as genetic counseling. A patient with characteristic symptoms of nevoid basal cell carcinoma and a review of the literature is presented.

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Published

2014-10-31

Issue

Section

Case Report

How to Cite

1.
Gorlin-Goltz syndrome: Case report. Int Jour of Biomed Res [Internet]. 2014 Oct. 31 [cited 2024 Oct. 18];5(10):659-61. Available from: https://ssjournals.co.in/index.php/ijbr/article/view/1100

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