首页 | 本学科首页   官方微博 | 高级检索  
检索        

多发性神经纤维瘤病的遗传规律及防治方法探讨
引用本文:墙华,彭亮,汪京峡.多发性神经纤维瘤病的遗传规律及防治方法探讨[J].宁夏医学杂志,2006,28(8):566-567.
作者姓名:墙华  彭亮  汪京峡
作者单位:1. 宁夏银川市第一人民医院,宁夏,银川,750001
2. 宁夏医学院,宁夏,银川,750004
3. 宁夏医学院附属医院,宁夏,银川,750004
摘    要:目的探讨多发性神经纤维瘤病遗传规律和防治方法。方法应用家系分析方法,对三个多发性神经纤维瘤病家系进行调查分析,用细胞遗传技术对8例患者和6例直系亲属的染色体核型进行分析。结果本病呈现连续世代遗传,男女均可发病,且机率均等;其染色体数目和结构均未见异常。结论本病为常染色体显性遗传病,对症治疗、手术切除恶性病变肿瘤、中药治疗和家系谱分析对NF1的预防和治疗是有应用价值的。

关 键 词:Ⅰ型神经纤维瘤病  遗传
文章编号:1001-5949(2006)08-0566-02
收稿时间:2006-04-10
修稿时间:2006年4月10日

Study on the genetic law, means of prevent and treatment for multipe neurofibromatosis(NF1)
QIANG Hua,et al.Study on the genetic law, means of prevent and treatment for multipe neurofibromatosis(NF1)[J].Ningxia Medical Journal,2006,28(8):566-567.
Authors:QIANG Hua  
Institution:The First Hosp. of Yinchuan, Ningxia 750001, China
Abstract:Objective To explore the genetic law,means of prevent and treatment for neurofibiomatosis(NF1).Methods The pidgree of 3 families were investigated,The karyotypies of 8 patients and 6 relatives were analyzed by using routine cytogeneties technique.Results The study showed that NF1 patients were found in every generation and there is no difference between genders among patients.NO aberration was found in the karyotypies of patients and their relatives.Conclusion Our results suggested that NF1 is an autosomal dominant disease,symptomatic treatment,neruofibrosacoma surgical removement,Chinese drugs and pedigrees analyzed are the useful means for prevented and treatment NF1.
Keywords:Type 1 neurofibromatosis  inheritance
本文献已被 CNKI 维普 万方数据 等数据库收录!
设为首页 | 免责声明 | 关于勤云 | 加入收藏

Copyright©北京勤云科技发展有限公司  京ICP备09084417号