A CASE REPORT OF GORLIN–GOLTZ SYNDROME AS A RARE HEREDITARY DISORDER (CASE REPORT)

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SIROUS MEHRI; TAYARI NAZILA

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Journal Paper

Paper Information

Journal: JOURNAL OF RESEARCH IN MEDICAL SCIENCES (JRMS) Year:2011 | Volume:16 | Issue:6 Page(s): 836-840

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Information Journal Paper

Title

A CASE REPORT OF GORLIN–GOLTZ SYNDROME AS A RARE HEREDITARY DISORDER (CASE REPORT)

Author(s)

SIROUS MEHRI | TAYARI NAZILA | Issue Writer Certificate

Keywords

KERATOGENIC CYST

FALX

TENTORIUM

GORLIN-GOLTZ SYNDROME

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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APA: Copy

SIROUS, MEHRI, & TAYARI, NAZILA. (2011). A CASE REPORT OF GORLIN–GOLTZ SYNDROME AS A RARE HEREDITARY DISORDER (CASE REPORT). JOURNAL OF RESEARCH IN MEDICAL SCIENCES (JRMS), 16(6), 836-840. SID. https://sid.ir/paper/591166/en

Vancouver: Copy

SIROUS MEHRI, TAYARI NAZILA. A CASE REPORT OF GORLIN–GOLTZ SYNDROME AS A RARE HEREDITARY DISORDER (CASE REPORT). JOURNAL OF RESEARCH IN MEDICAL SCIENCES (JRMS)[Internet]. 2011;16(6):836-840. Available from: https://sid.ir/paper/591166/en

IEEE: Copy

MEHRI SIROUS, and NAZILA TAYARI, “A CASE REPORT OF GORLIN–GOLTZ SYNDROME AS A RARE HEREDITARY DISORDER (CASE REPORT),” JOURNAL OF RESEARCH IN MEDICAL SCIENCES (JRMS), vol. 16, no. 6, pp. 836–840, 2011, [Online]. Available: https://sid.ir/paper/591166/en

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