检索规则说明:AND代表“并且”;OR代表“或者”;NOT代表“不包含”;(注意必须大写,运算符两边需空一格)
检 索 范 例 :范例一: (K=图书馆学 OR K=情报学) AND A=范并思 范例二:J=计算机应用与软件 AND (U=C++ OR U=Basic) NOT M=Visual
作 者:李鹏 陈志鹏[2] 林立强[2] 陈庆泳 吕怀庆[2]
机构地区:[1]山东第二医科大学临床医学院,山东 潍坊 [2]临沂市人民医院耳鼻咽喉头颈外科,山东 临沂
出 处:《临床医学进展》2024年第7期12-18,共6页Advances in Clinical Medicine
摘 要:先天性唇瘘是一种极其罕见的先天性畸形,大多发生在下唇,发生在上唇者少见。患者多因局部不适或美容需求而就诊,由于先天性唇瘘畸形发生率极低,且部分患者无明显临床表现,往往容易被患者或临床医生忽视,但该畸形可与多种罕见的遗传性疾病相关联,临床医生认识该畸形对于为患者提供更好的治疗方式和可能的遗传咨询具有重要意义。本文就这先天性唇瘘的流行病学、临床表现、解剖特征、相关疾病和治疗方法等进行综述。Congenital lip sinus is a rare congenital deformity, predominantly occurring in the lower lip with less frequency in the upper lip. Patients often seek medical attention due to local discomfort or concerns about appearance. Due to its low incidence rate and the fact that some patients may lack obvious clinical manifestations, this condition is often overlooked. However, congenital lip sinus can be associated with various genetic diseases. Understanding this anomaly is of paramount importance for providing better treatment options and possible genetic counseling for patients. This article reviews the relevant research progress.
正在载入数据...
正在载入数据...
正在载入数据...
正在载入数据...
正在载入数据...
正在载入数据...
正在载入数据...
正在链接到云南高校图书馆文献保障联盟下载...
云南高校图书馆联盟文献共享服务平台 版权所有©
您的IP:3.139.239.16