接受正畸治疗的兄弟姐妹的Silver-Russell综合征

Vijaylaxmi B Mendigeri, Praveenkumar Ramdurg, Fatima Lingadalli, Sanjay V. Ganeshkar
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引用次数: 0

摘要

银罗素综合征(SRS)是一种罕见的先天性异常。发病率从每3000例活产1例到10万例活产1例。其特点是出生体重低,肢体不对称,相对大头畸形,前额高,小三角形脸,下颌小,牙错合。SRS的病因尚不清楚,但遗传改变和家族史已被归因于。SRS的诊断主要基于身体特征和外观。本文对两兄弟姐妹的SRS的临床多功能性进行了启发,并讨论了老年人牙齿错颌的正畸治疗。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Silver–Russell syndrome in siblings with orthodontic management
Silver–Russell syndrome (SRS) is a rare congenital abnormality. The incidence ranges from 1 in 3000 to 100,000 live births. It is characterized by low birth weight, asymmetric limb, relative macrocephaly, high forehead, small triangular-shaped face with small jaws, and dental malocclusion. The etiology of SRS is still unclear, but genetic alterations and family history have been attributed. The diagnosis of SRS is mainly based on physical characteristics and appearance. This article enlightens clinical versatility in dental features of SRS in two siblings and discusses the orthodontic management for dental malocclusion in the elder one.
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