Ey-Chmielewska Halina, Sobolewska Ewa, Fraczak Bogumiła
Zakład Protetyki Stomatologicznej Pomorskiej Akademii Medycznej w Szczecinie, Szczecin.
Ann Acad Med Stetin. 2007;53(2):83-6.
Neurofibromatosis is a hereditary autosomal predominating disease occuring in one out of every 2000 or 3300 alive births. The classical form of neurofibromatosis was described by von Recklinghausen in 1882. The disease is a gene mutation, where the anomalies affect mesoderm and neuroectoderm. The paper presents the therapeutic treatment method for the case of lacking teeth restoration in a patient diagnosed with known form ofneurofibromatosis NF-1 in Recklinghausen disease.
神经纤维瘤病是一种常染色体显性遗传性疾病，每2000至3300例活产婴儿中就有1例发病。神经纤维瘤病的经典形式由冯·雷克林豪森于1882年描述。该疾病是一种基因突变，异常影响中胚层和神经外胚层。本文介绍了对一名被诊断患有冯·雷克林豪森病中已知形式的神经纤维瘤病NF-1患者牙齿缺失修复的治疗方法。
