Tewari S, Govila C P, Garg A P
Department of Operative Dentistry, K. G.'s Medical College Lucknow, India.
J Oral Pathol Med. 1991 Nov;20(10):514-5. doi: 10.1111/j.1600-0714.1991.tb00416.x.
Rieger's syndrome which is a congenital progressive, autosomally dominant, ophthalmic anomaly has certain associated somatic dentofacial and systemic features. These extra dentofacial and systemic findings can play very important role in diagnosing this syndrome so as to prevent the ocular complications. This article reports such a case in a 20-yr-old woman and discusses somatic features along with the clinical importance of early diagnosis.
里格尔综合征是一种先天性进行性常染色体显性遗传的眼部异常疾病，伴有某些相关的躯体、牙颌面及全身特征。这些额外的牙颌面及全身表现对于该综合征的诊断起着非常重要的作用，有助于预防眼部并发症。本文报道了一名20岁女性的此类病例，并探讨了躯体特征以及早期诊断的临床重要性。
