Mulvihill–Smith syndrome: A case report

Kaori Yago , Taneaki Nakagawa , Tomoko Hyodo , Kenjiro Kosaki , Yusuke Kawata , Youichi Tanaka , Soichiro Asanami
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引用次数: 2

Abstract

Mulvihill–Smith syndrome (MSS) is a very rare disease that is characterized by short stature, a senile face with an under-developed lower half, microcephaly, multiple pigmented nevi, immunodeficiency, hearing loss, and high-pitched voice. We report on the oral manifestations and management of a 27-year-old woman with this syndrome, who underwent removal of a mandibular cyst and partial resection of the tongue.

Mulvihill-Smith综合征1例报告
Mulvihill-Smith综合征(MSS)是一种非常罕见的疾病,其特征是身材矮小,面部衰老,下半身发育不全,小头畸形,多发性色素痣,免疫缺陷,听力丧失和高音。我们报告的口腔表现和管理27岁的妇女与这种综合征,谁接受下颌囊肿切除和部分切除舌头。
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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