A Case Report of Gorlin-Goltz Syndrome As a Rare Hereditary Disorder

A Case Report of Gorlin-Goltz Syndrome As a Rare Hereditary Disorder

Sirous M¹ ; Tayari N¹

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1. Department of Radiology, Isfahan University of Medical Sciences, Isfahan, Iran

Source: Journal of Research in Medical Sciences Published:2011

Abstract

Gorlin-Goltz syndrome is an autosomal dominant and a rare hereditary disease. Diagnosis of this syndrome is based on major and minor criteria. We report a Gorlin-Goltz syndrome in a 25-year-old male who was presented with progressive pain of maxilla and mandible over 5 years. The pain was diffuse and compatible with expansile cyst in alveolar ridges on panoramic radiography. In physical examination, he had coarse face and prognathism. Computer tomography of face revealed two expansile maxillary and one mandibular cyst. Calcification of entire length in falx and tentorium were detected in bone window.

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Style	Citing Format
MLA	Sirous M, Tayari N. "A Case Report of Gorlin-Goltz Syndrome As a Rare Hereditary Disorder." Journal of Research in Medical Sciences, vol. 16, no. 6, 2011, pp. 836-840.
APA	Sirous M, Tayari N (2011). A Case Report of Gorlin-Goltz Syndrome As a Rare Hereditary Disorder. Journal of Research in Medical Sciences, 16(6), 836-840.
Chicago	Sirous M, Tayari N. "A Case Report of Gorlin-Goltz Syndrome As a Rare Hereditary Disorder." Journal of Research in Medical Sciences 16, no. 6 (2011): 836-840.
Harvard	Sirous M, Tayari N (2011) 'A Case Report of Gorlin-Goltz Syndrome As a Rare Hereditary Disorder', Journal of Research in Medical Sciences, 16(6), pp. 836-840.
Vancouver	Sirous M, Tayari N. A Case Report of Gorlin-Goltz Syndrome As a Rare Hereditary Disorder. Journal of Research in Medical Sciences. 2011;16(6):836-840.
BibTex	@article{ author = {Sirous M and Tayari N}, title = {A Case Report of Gorlin-Goltz Syndrome As a Rare Hereditary Disorder}, journal = {Journal of Research in Medical Sciences}, volume = {16}, number = {6}, pages = {836-840}, year = {2011} }
RIS	TY - JOUR AU - Sirous M AU - Tayari N TI - A Case Report of Gorlin-Goltz Syndrome As a Rare Hereditary Disorder JO - Journal of Research in Medical Sciences VL - 16 IS - 6 SP - 836 EP - 840 PY - 2011 ER -

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