一名12岁女孩患丹迪-沃克综合征的罕见病例。
A rare case of Dandy-Walker syndrome in the 12-year-old girl.
作者信息
Khandelwal Deepak, Kumar Dhiraj, Kalra Namita, Tyagi Rishi, Khatri Amit, Kumar Sunil
机构信息
Department of Pedodontics and Preventive Dentistry, University College of Medical Sciences (University of Delhi) and GTB Hospital, New Delhi, India.
出版信息
J Indian Soc Pedod Prev Dent. 2020 Jan-Mar;38(1):94-96. doi: 10.4103/JISPPD.JISPPD_343_18.
Dandy-Walker syndrome (DWS) is a rare congenital cystic malformation of the posterior cranial fossa. Patients show signs and symptoms of complex clinical manifestations, ranging from cranial nerve and cerebellar dysfunctions to extracranial abnormalities, which may pose challenges in dental management. This article represents a rare case of a 12-year-old girl with DWS along with the involvement of the oral cavity.
丹迪-沃克综合征（DWS）是一种罕见的先天性后颅窝囊性畸形。患者表现出复杂的临床表现体征和症状，从颅神经和小脑功能障碍到颅外异常，这可能给牙科治疗带来挑战。本文报道了一例罕见的12岁丹迪-沃克综合征女童病例，该病例还累及口腔。
Zotero 插件