GORLIN SYNDROME

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SHIRZAII MASOOMEH; RISBAF SIROOS

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Journal Paper

Paper Information

Journal: Zahedan Journal of Research in Medical Sciences Year:2013 | Volume:15 | Issue:1 Page(s): 60-62

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Information Journal Paper

Title

GORLIN SYNDROME

Author(s)

SHIRZAII MASOOMEH | RISBAF SIROOS | Issue Writer Certificate

Keywords

GORLIN SYNDROME

BASAL CELL CARCINOMA

JAW CYST

Abstract

GORLIN SYNDROME is a dominant autosomal familial disorder. The manifestations begin at an early age and a combination of phenotypic abnormalities such special facial appearance, JAW CYSTs and skeletal anomalies are seen in this disease. A 22-year-old woman referred to Zahedan Dental School complaining of pain on the left cheek. During the examination, several cutaneous lesions in the neck, pits in palm and sole and multiple JAW CYSTs were observed. According to the clinical symptoms, lesion biopsy and reports of GORLIN SYNDROME radiography were presented.

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APA: Copy

SHIRZAII, MASOOMEH, & RISBAF, SIROOS. (2013). GORLIN SYNDROME. ZAHEDAN JOURNAL OF RESEARCH IN MEDICAL SCIENCES (TABIB-E-SHARGH), 15(1), 60-62. SID. https://sid.ir/paper/619634/en

Vancouver: Copy

SHIRZAII MASOOMEH, RISBAF SIROOS. GORLIN SYNDROME. ZAHEDAN JOURNAL OF RESEARCH IN MEDICAL SCIENCES (TABIB-E-SHARGH)[Internet]. 2013;15(1):60-62. Available from: https://sid.ir/paper/619634/en

IEEE: Copy

MASOOMEH SHIRZAII, and SIROOS RISBAF, “GORLIN SYNDROME,” ZAHEDAN JOURNAL OF RESEARCH IN MEDICAL SCIENCES (TABIB-E-SHARGH), vol. 15, no. 1, pp. 60–62, 2013, [Online]. Available: https://sid.ir/paper/619634/en

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