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Case Reports
. 2009 Jul;13(2):89-92.
doi: 10.4103/0973-029X.57677.

Gorlin-Goltz syndrome

Deepti Singh Jawa  1 , Keya Sircar, Rani Somani, Neeraj Grover, Shipra Jaidka, Sanjeet Singh
Affiliations
Case Reports

Gorlin-Goltz syndrome

Deepti Singh Jawa et al. J Oral Maxillofac Pathol. 2009 Jul.

Abstract

Gorlin-Goltz syndrome is an autosomal dominant inherited disorder characterized by the presence of multiple odontogenic keratocysts along with various cutaneous, dental, osseous, ophthalmic, neurological, and sex organ abnormalities. Early diagnosis is essential as it may progress to aggressive basal cell carcinomas and neoplasias. Gorlin-Goltz syndrome has rarely been reported from India. We report here one such patient, diagnosed at a rural hospital.

Keywords: Diagnosis; Gorlin-Goltz syndrome; odontogenic keratocyst.

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Conflict of interest statement

Conflict of Interest: None declared.

Figures

Figure 1
Figure 1
Sebaceous cyst over middle finger of the left hand
Figure 2
Figure 2
Sebaceous cyst on the back
Figure 3
Figure 3
Accessory toe with syndactily with 5th digit of right foot
Figure 4
Figure 4
Orthopantogram showing bilateral cyst with unerupted teeth
Figure 5
Figure 5
Chest X-ray showing bifid rib
Figure 6
Figure 6
Biopsy from right mandibular lesion showing odontogenic keratocyst showing characteristic cystic epithelial lining (H and E, ×10)
See this image and copyright information in PMC

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