戈尔茨戈林综合征1例报告及综述

Dr. Prasanna Kumar D., Dr. Nidhi Jenson Ukken, Dr. H K Ajeya Ranganathan, Dr. Mohammed Basim, Dr.Mariea Francis, Dr. Vijay Joseph Chethalan
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引用次数: 0

摘要

戈尔茨-戈林综合征(GGS)是一种多系统疾病,常染色体显性遗传病,具有完全变异,尽管有不规则病例的描述。本文包括一个病例报告和对GGS的历史、发病率、病因、特征、调查、诊断标准、角化囊性牙源性肿瘤和治疗方式的广泛回顾。一位32岁的女性患者,表现出Gorlin-Goltz综合征的三个主要特征。该综合征的放射学表现在骨断层扫描、ct扫描上很容易识别。这些调查提示疾病的早期验证,这对于防止复发和提高共存疾病的生存率非常重要。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
GOLTZ GORLIN SYNDROME- A CASE REPORT WITH OVERVIEW
Goltz Gorlin syndrome (GGS) is an multisystemic disease with an autosomal dominant disorder, with complete variance, though irregular cases have been described. This article includes a case report and an extensive review of the GGS with regard to its history, incidence, etiology, features, investigations, diagnostic criteria, keratocystic odontogenic tumor and treatment modalities. case of a 32-year-old female patient presenting with three major features of Gorlin-Goltz syndrome. Radiologic findings of the syndrome are easily identifiable on Orthopantomogram, cbct scans. These investigations prompt an early verification of the disease, which is very important to prevent recurrence and better survival rates from the coexistent diseases.
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