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首页> 外文期刊>The journal for nurse practitioners: JNP >Neurofibromatosis 1: Diagnosis and management
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Neurofibromatosis 1: Diagnosis and management

机译:神经纤维瘤病1:诊断和处理

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摘要

Von Recklinghausen or neurofibromatosis type 1 is an autosomal dominant condition that results in skin changes and noncancerous tumors along the nerves in the body. It is blind in regards to ethnicity, race, or sex. With a prevalence rate of 1 in 3,000 to 1 in 3,500 individuals, it is likely that the nurse practitioner will encounter an individual with neurofibromatosis sometime in his/her career. The aim of this article is to give a brief synopsis of the etiology, clinical manifestations, and symptomatic treatment as well as guidance on monitoring, when to refer, health promotion, and teaching of the neurofibromatosis type 1 patient.
机译:冯·瑞克林豪森或1型神经纤维瘤病是常染色体显性疾病,会导致皮肤变化和沿人体神经的非癌性肿瘤。在种族,种族或性别方面是盲目的。患病率为3,000人中有1人至3500人中有1人,因此护士从业者很可能会在某个时间遇到神经纤维瘤病患者。本文的目的是简要概述1型神经纤维瘤病患者的病因,临床表现和对症治疗以及监测,何时转诊,促进健康和教学的指导。

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