阿斯科格-斯科特综合征患者的牙面特征

IF 0.5 Q4 DENTISTRY, ORAL SURGERY & MEDICINE Orthodontic Waves Pub Date : 2018-06-01 DOI:10.1016/j.odw.2018.03.001

Chihiro Tanikawa , Hiroshi Kurosaka , Kohei Nakatsugawa , Takashi Yamashiro

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引用次数: 0

摘要

Aarskog-Scott综合征(ASS)，也被称为面部-手指-生殖器综合征或面部-生殖器发育不良，是一种罕见的X-linked隐性遗传病，主要影响男性个体的肌肉骨骼系统，与FGD1突变有关。本研究报告一名九岁日本男童在三岁时被诊断为ASS。该患者就诊于我们的正畸科，表现为牙缺损、阻生牙、延迟出牙、上弓狭窄和下颌后突。在本报告中，我们介绍了患者的牙面特征。

本文章由计算机程序翻译，如有差异，请以英文原文为准。

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Dentofacial characteristics in a patient with Aarskog–Scott syndrome

Aarskog–Scott syndrome (ASS), also known as facio-digito-genital syndrome or faciogenital dysplasia, is a rare X-linked recessive disorder that mainly affects the musculoskeletal system of male individuals, and is related with mutations in FGD1. This study presents the case of a 9-year old Japanese boy who was diagnosed with ASS at the age of three. The patient presented to our orthodontic department with hypodontia, impacted teeth, and delayed eruption, with narrow upper arch and retrognathic mandibles. In the present report, we introduce the patient’s dentofacial characteristics.

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来源期刊

Orthodontic Waves DENTISTRY, ORAL SURGERY & MEDICINE-

CiteScore

0.40

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0.00%

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期刊介绍： Orthodontic Waves is the official publication of the Japanese Orthodontic Society. The aim of this journal is to foster the advancement of orthodontic research and practice. The journal seeks to publish original articles (i) definitive reports of wide interest to the orthodontic community, (ii) Case Reports and (iii) Short Communications. Research papers stand on the scientific basis of orthodontics. Clinical topics covered include all techniques and approaches to treatment planning. All submissions are subject to peer review.