关键词: axenfeld-rieger syndrome craniofacial anomalies genetic glaucoma ocular axenfeld-rieger syndrome craniofacial anomalies genetic glaucoma ocular

来  源:   DOI:10.7759/cureus.26442   PDF(Pubmed)

Abstract:
Axenfeld-Rieger syndrome (ARS) is an autosomal dominant syndrome with a prevalence estimated at 1:50000 to 1:100000 in newborns. It is mainly characterized by ocular, craniofacial, and dental abnormalities. From the pediatric dentist\'s point of view, early diagnosis of the syndrome from the ocular, craniofacial, and dental manifestation can prevent further abnormalities and ocular complications such as glaucoma. This case report presents a brief description of ARS with the characteristics of craniofacial and dental findings.
摘要:
Axenfeld-Rieger综合征(ARS)是一种常染色体显性综合征,在新生儿中的患病率估计为1:50000至1:100000。它的主要特点是眼,颅面,和牙齿异常。从儿科牙医的角度来看,从眼部早期诊断,颅面,和牙齿表现可以防止进一步的异常和眼部并发症,如青光眼。此病例报告简要介绍了具有颅面和牙齿发现特征的ARS。
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