A case report of Gorlin–Goltz syndrome as a rare hereditary disorder

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 an...

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Detalles Bibliográficos
Autores principales: Sirous, Mehri, Tayari, Nazila
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Medknow Publications Pvt Ltd 2011
Materias:
Case Report
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3214404/
https://www.ncbi.nlm.nih.gov/pubmed/22091315
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author Sirous, Mehri
Tayari, Nazila
author_facet Sirous, Mehri
Tayari, Nazila
author_sort Sirous, Mehri
collection PubMed
description 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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spelling pubmed-32144042011-11-16 A case report of Gorlin–Goltz syndrome as a rare hereditary disorder Sirous, Mehri Tayari, Nazila J Res Med Sci Case Report 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. Medknow Publications Pvt Ltd 2011-06 /pmc/articles/PMC3214404/ /pubmed/22091315 Text en Copyright: © Journal of Research in Medical Sciences http://creativecommons.org/licenses/by-nc-sa/3.0 This is an open-access article distributed under the terms of the Creative Commons Attribution-Noncommercial-Share Alike 3.0 Unported, which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Case Report
Sirous, Mehri
Tayari, Nazila
A case report of Gorlin–Goltz syndrome as a rare hereditary disorder
title A case report of Gorlin–Goltz syndrome as a rare hereditary disorder
title_full A case report of Gorlin–Goltz syndrome as a rare hereditary disorder
title_fullStr A case report of Gorlin–Goltz syndrome as a rare hereditary disorder
title_full_unstemmed A case report of Gorlin–Goltz syndrome as a rare hereditary disorder
title_short A case report of Gorlin–Goltz syndrome as a rare hereditary disorder
title_sort case report of gorlin–goltz syndrome as a rare hereditary disorder
topic Case Report
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3214404/
https://www.ncbi.nlm.nih.gov/pubmed/22091315
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