神经遗传病介绍PPT课件

.,1,第十六章神经系统遗传病,GeneticDiseaseoftheNervousSystemDepartmentofNeurologySecondAffiliatedHospitalHarbinMedicalUniversity,.,2,Geneticdiseaseofnervoussystem1、Introduction2、FriedreichAtaxia3、SpinocerebellarAtaxia(SCA)4、Charcot-Marie-ToothDisease掌握：1、Friedreich型共济失调的主要临床特征、临床表现。2、脊髓小脑性共济失调的临床表现、诊断及鉴别诊断。,.,3,熟悉：1、Friedreich型共济失调的病因、发病机制。2、脊髓小脑性共济失调的病因、发病机制。3、腓骨肌萎缩症(CMT)的临床表现、诊断及鉴别诊断。,.,4,第一节GeneralIntroduction,1.ConceptionGeneticdiseaseofthenervoussystem是指由于生殖细胞（germcell）或受精卵（zygote）中的遗传物质在数量、结构或功能上发生改变，使发育的个体出现以神经系统缺欠(deficiency)为主要临床表现的疾病。CongenitalDiseaseFamilyDisease,.,5,ClassificationandGeneticpattern,MonogenicDisordersPolygenicDisordersMitochondrialDisordersChromosomeDisorders,.,6,1.Monogenicdisorders：Thebasereplacement,Insert,Deletion,repeatorabnormalexpansionofsinglegene.AutosomaldominantdisordersAutosomalrecessivedisordersX-linkeddominantdisordersX-linkedrecessivedisorders动态突变性遗传CommonDiseases:Charcot-Marie-Tooth,Duchennemusculardystrophy,WilsonDisease,HereditaryAtaxia,.,7,2.polygenicdisorders:areinfluencedbygenesincomplexwayswhicharepoorlyunderstoodbutinvolvetheinteractionofmultiplegenesandinteractionsbetweengenesandenvironmentalfactorsThecommonpolygenicdisorders:Epilepsy,migraineandarteriosclerosis.,.,8,3.线粒体遗传病(mitochondrialdisorders)Mitochondrialdisordersarecausedbymutationofmitochondrion(numberorstructure)，Theyarematernalinheritance.opticatrophyandmitochondrialencephalomyopathy.4.ChromosomedisordersChromosomedisordersarecausedbythenumberorconstructionabnormalitiesofchromosome.forexample：Downsyndrome,.,9,Symptomsandphysicalsigns,Clinicalfeaturesareofdiversity,includecommonandspecificsymptomsCommonsymptoms:Specificsymptoms,.,10,1.Commonsymptoms:MentalretardationandDisturbanceofbehaviorLanguagedysfunction,dementiaSeizure、Nystagmus,Paraesthesia(感觉异常)Involuntarymovement(不自主运动)、AtaxiaandDystonia(肌张力障碍)Muscleatrophy还可有五官畸形、脊柱裂、弓型足、指（趾）畸形、皮肤毛发异常和肝脾肿大；,.,11,2.Specificsymptom：肝豆状核变性K-F环、共济失调毛细血管扩张症结合膜毛细血管扩张结节性硬化症面部皮脂腺瘤神经纤维瘤皮肤牛奶咖啡斑,.,12,.,13,.,14,.,15,.,16,4.Diagnosis:(1).临床资料的搜集：尤其是发病年龄、性别、独特的症状和体征，如牛奶咖啡斑(2).系谱分析(pedigreeanalysis)可判断有无遗传病和区分类型(3).常规辅助检查:Includebiochemistry,Electrophysiology,ImagingstudiesandPathology对诊断和鉴别诊断具有重要意义，如：假肥大型肌营养不良血清学；肝豆状核变性血清铜兰蛋白、血清铜和尿铜;腓骨肌萎缩症神经活检;脊髓小脑性共济失调,橄榄脑桥小脑萎缩的头颅MRI;,.,17,(4).geneticdiagnosis：1)染色体检查(karyotypeanalysis)：染色体数目异常；染色体结构畸变(constructiveaberration):2)基因诊断(genedetection)：方法包括:SouthernHybridization，PCR3)Geneproductiondetection：假性肥大肌营养不良-测定肌细胞膜上抗肌萎缩蛋白(dystrophin),.,18,5.treatmentandPreventionNoeffectivetreatment基因治疗(genetherapy)是指应用基因工程技术来更换、校正或增补基因，以达到治疗遗传病的目的，但目前基因治疗还很不成熟；其他治疗包括：Operation;medicinetherapy；Diettherapy；symptomtherapy;rehabilitation。,.,19,Prevention：important遗传咨询（geneticcounseling)；避免近亲结婚；携带者检测(carrierdetection)；产前诊断；选择性人工流产(selectiveabortion)；,.,20,第二节hereditaryataxia,1.Conception：HereditaryataxiaisagroupofinheritedanddegenerativedisordersofCNS.Characterizedbyslowlyprogressiveataxia.Thesedisordersshowconsiderableclinicvariability.But,geneticbackground,ataxiaandspinocerebellarlesionaremainlyclinicalfeaturesofthem.,.,21,2.Classification:Traditionalclassificationbypathologicfindings:SpinalAtaxia;SpinocerebellarAtaxia;Cerebellarataxia;Newclassificationbytheonsetofage,clinicalfeatures,Geneticpatternandlocationofgenemutation（参考表16-1）byHarding(1993)p.270,.,22,Friedreich型共济失调Friedreichreportthisdiseasefirstlyin1863，Itsincidencerateis2/100000，Itisaearly-onsetataxiaandtransmittedbyautosomalrecessiveinheritance,.,23,1.EtioligyandPathogenesisFriedreichataxia(FRDA)是由位于9号染色体长臂(9q13-21.1)基因缺陷所致。95%以上的病人有该基因第18号内含子(intron)GAA异常扩增（661700次），正常人GAA重复42次以下，扩增的GAA形成的异常螺旋结构可抑制基因转录(genetranscription)。Friedreich共济失调的基因产物Frataxin蛋白主要位于spinalcord、Skeletonmuscle、heartandliver细胞线粒体(mitochondrion)的内膜，可导致线粒体功能障碍而发病。,.,24,2.PathologyPosteriorcolumnsandlateralcolumnofspinalcordaremainlyinvolved，thespinalcordisthin，especiallyinthoracalspinalcord。Microscopecanfindthatcelllossofposteriorcolumn,spinocerebellartract,pyramidaltractdegenerate,dorsalrootgangliaandClarkescolumn；peripheralnervedemyelinationandgliosis；brainstem、cerebellumandbrainarerarelyinvolved；Cardiomyopathyandheartcellhypertrophy。,.,25,3.clinicalfindings(1)Theageofonsetis8-15yearsoldercommonly,withmoreexpandedrepeatscorrelatingwithearlieronset。(2).Theinitialsymptomisprogressivegaitataxia,followedbyataxiaofalllimbswithin2years.usually,bothlegsareaffectedsimultaneously,difficultyinstandingandwalkingsteadily；thehandsusuallybecomeclumsymonthoryearsafterthegaitdisorderwithintentiontremor；Dysarthricspeechappearsafterthearmsareinvolved(rarelyisthisanearlysymptom)。,.,26,(3)Physicalexamination:可见水平眼震(horizontalnystagmus)，垂直性(vertical)和旋转性(rotatory)眼震较少;双下肢肌无力，肌张力低(muscletonedecreased)，跟膝胫试验(Heel-knee-shin)和闭目难立征(Rombergsign)阳性；下肢音叉震动觉(vibrationsense)和关节位置觉(jointpositionsense)减退是早期体征；后期可有Babinskisign,Muscleatrophy，occasionally,sphincterdistubances；,.,27,约25%患者有视神经萎缩(opticatrophy);75%有上胸段脊柱侧(kyphoscoliosis)，50%有弓形足(pescavus)；85%有心律紊乱、心脏杂音；10%20%伴有糖尿病(diabetes)。(4)通常起病15年后卧床（bedridden），多于4050岁死于感染或心脏病。,.,28,4.investigativestudies(1).skeletonfilmshowskeletalabnormalities；CT或MRI示脊髓变细，cerebellumandbrainstemarerarelyinvolved；(2).心电图(electrocardiograph):常有T波倒置、心律紊乱及传导阻滞；(3).Echocardiography:Hypertrophy；(4).视诱发电位(visualevokedpotential):Amplitudedecreased；(5).脑脊液(cerebrospinalfluid):normalprotein；(6).DNA分析FRDA基因18号内含子GAA大于66次重复。,.,29,5.Diagnosisanddifferentialdiagnosis(1).Diagnosis:Earlyonset;SlowlyProgressiveAtaxiafrombothlegstoarms;Dysarthria,Nystagmus,tendonreflexabsentandBabinskisign；lossofvibratoryandjointpositionsense;Kyphoscoliosis，Pesvacus，heartlesion;MRI显示脊髓萎缩，则不难诊断;FRDA基因GAA异常扩增，可确定诊断。,.,30,(2)不典型病例需与其他疾病鉴别慢性变性疾病和脱髓鞘性疾病(demyelinativedisease),Charcot-Marie-ToothDisease；还应与VitE缺乏和-脂蛋白缺乏引起的共济失调鉴别，后两者可查血清VitE和-脂蛋白的含量以鉴别之。6.treatmentnoeffectivetreatmentisavailable，轻症病人给予支持疗法，康复(rehabilitation)治疗；重症者可手术矫治弓形足等畸形；用胞二磷胆碱、毒扁豆碱可能有一定的疗效。,.,31,脊髓小脑性共济失调（SpinocerebellarataxiaSCA）SCA是遗传性共济失调的主要类型，包括SCA1-10.Thecommonfeature:onsetinmiddlelife、autosomaldominanthereditaryandataxia.Harding根据有无眼肌麻痹(ophthalmoplegia)、锥体外系(extrapyramidal)症状及视网膜色素变性(retinalpigmentdegeneration)归纳为三组十个亚型(表16-1)，SCA的发病与种族有关，SCA1-2在意大利、英国多见，中国、德国和葡萄牙以SCA3最常见。,.,32,1.etiologyandpathogenesisSCA有共同的突变机制，即相应的基因外显子(exon)CAG拷贝数异常扩增,产生多聚谷氨酰胺链(SCA8除外)，产生毒性功能，共同的突变机制也是造成SCA各亚型的临床表现雷同的原因。然而，每一SCA亚型的基因位于不同的染色体，其基因大小及突变部位均不相同（见16-1表），SCA各亚型的临床表现也有差异，如有的伴有眼肌麻痹(ophthalmoplegia)，有的伴有视网膜色素变性，病理损害的部位和程度也有所不同，这提示除了多聚谷氨酰胺毒性作用之外，可能还有其它因素参与发病。,.,33,2.pathologyThecommonpathologicallesionofSCAisincerebellum、brainstem，withthedegenerativespinalcord.但各亚型也有其特点，如：SCA1:lossofneuroninbrainstemandcerebellum，spinocerebellartractandposteriorcolumnareusuallyinvolved，很少累及黑质（blackmatter）、basalgangliaandanteriorcorncell；SCA2:nucleiofinferiorolivary.Ponsandcerebellum；SCA3:pontineandspinocerebellartractSCA7:Retinalneurondegeneration。,.,34,3.clinicalfindingsSCA是高度遗传异质性疾病，各亚型的症状相似，交替重叠，其共同临床表现是：(1).一般在3040岁隐袭起病，缓慢进展，但也有儿童期及70岁起病者。(2).首发症状多为下肢共济失调，走路摇晃、突然跌倒、发音困难；继而出现双手笨拙及意向性震颤(intentiontremor);可见眼震,眼慢扫视运动阳性,dementiaanddistalmuscleatrophy；Dystonia,increasedtendonreflex,pathologicalreflex,spasticgaitandsenseofvibrationandproprioceptionabsent。,.,35,(3).均有遗传早现现象，即在同一SCA家系中发病年龄逐代提前，症状逐代加重，是SCA非常突出的表现。一般起病后1020年患者不能行走。(4).除了上述共同的症状和体征外，各亚型也具各自的特点而构成不同的疾病。如SCA1的眼肌麻痹(ophthalmoplegia)，尤其上视不能较突出；SCA2的上肢腱反射减弱或消失，眼慢扫视运动较明显；SCA3的肌萎缩、面肌(facial)及舌肌(glossal)纤颤(fasciculation)、眼睑退缩形成凸眼；,.,36,SCA5病情进展非常缓慢，症状也较轻；SCA6的早期大腿肌肉痉挛(spasm)、下视震颤、复视(diplopia)和位置性眩晕(vertigo)；SCA7的特征性症状是视力减退或丧失，视网膜色素变性，心脏损害也较突出;SCA8常有发音困难(dysarthria)；SCA10的纯小脑征和癫(epilepsy)发作;,.,37,4.Labstudies(1).CTorMRshowcerebellarandbrainstematrophy，especiallyponsandthemiddlepeduncleofcerebellumatrophy;(2).brainstemevokedpotentialmaybeabnormal;(3).Electromyographyshowperipheralnervelesion；(4).normalcerebrospinalfluid；(5).确诊及区分亚型可用外周血白细胞进行PCR分析，检测相应基因CAG扩增的情况;,.,38,5.diagnosisanddifferentialdiagnosis根据典型的共性症状；结合(magneticresonanceimagingMRI)检查发现小脑、脑干萎缩；排除其它累及小脑和脑干的变性病即可确诊;基因诊断确定其亚型及CAG扩增次数是确诊的goldenstandard。,.,39,不典型病例需与多发性硬化(multiplesclerosis)、CJD及感染引起的共济失调鉴别。6.treatmentNospecifictreatmentavailableuntilnow.对症及康复治疗可缓解症状。,.,40,第三节腓骨肌萎缩症(Charcot-Marie-ToothDiseaseCMT)Introduction:CMTorhereditarymotorsensoryneuropathy(HMSN).Charcot.MarieandToothreportitfirstlyin1886,Itisthemostcommontypeofhereditarymotorsensoryneuropathy.theincidencerateis1/2500。,.,41,Classification:I型:nerveconductionvelocitylessthan38cm/s.include3subtypes1A,1Band1Cbygenelocation.II型:nerveconductionvelocitynormalornearlynormal。Include4subtypes:2A、2B、2Cand2D.以CMT1A型最常见。,.,42,1.etiologyandpathologenesisThemajorityofCMTisautosomaldominantheredity，Theminorityofitistransmittedbyotherhereditarypatterns.(1).CMT1A：致病基因定位于17p11.2-12，该基因编码周围神经髓鞘蛋白22(PMP22)，它的重复突变导致PMP22基因过度表达(over-expression)，使周围髓鞘蛋白(myelinprotein)增加；另有一小部分病人因周围神经髓鞘蛋白PMP22基因的点突变，产生异常PMP22蛋白而致病；(2).CMT2型：autosomaldominantheredity，与其有关的基因至少定位于三个位点,分别位于1,3,7号染色体上.,.,43,2.PathologyTheaxonandmyelinsheathsofperipheralnerveareinvolved，thedistalpartsofnervemorethantheproximal。I型神经纤维呈对称性节段性脱髓鞘，部分髓鞘再生，Schwann细胞增生与修复，形成“洋葱头”(onion-bulb)样结构，造成运动和感觉神经传导速度减慢II型为轴突变性(axondegeneration)，运动和感觉神经传导速度改变不明显；前角细胞(anteriorhorncell)数量轻度减少，Themusclesoccurgroupatrophy(簇状萎缩)。当累及感觉后根纤维时，薄束变性比楔束更严重；theautosomalnervoussystemremainsrelativelyintact。,.,44,3.clinicalfindingsCMTI型(脱髓鞘型)：(1)theageofonsetislatechildhoodandadolescence.thesymmetricalchronicdegenerationofperipheralnerveresultindistalmuscleatrophy，多数患者开始是足和下肢，数月至数年可波及到手肌和前臂肌，extensorsareinvolvedearly,Flexorisnormal,产生马蹄内翻足和爪形足(clawfoot)畸形，footdrop及跨阈步态。常伴有脊柱侧弯。,.,45,(2)检查可见受累肢体肌肉萎缩，小腿肌肉和大腿的下1/3肌肉(thelowerthirdofthethighmuscleweakandatrophy)，justlikestorklegorinvertedchampagnebottle，手肌萎缩，并波及前臂肌肉，变成爪形手。很少波及肘以上部分;Thetendonreflexareabsentintheinvolvedlimbs；深浅感觉减退可从远端开始，呈手套、袜子样分布；伴有自主神经功能障碍和营养代谢障碍，Rarely,thesensorylossissevere,andperforatingulcersmayappear。,.,46,(3)病程非常缓慢，在很长时期内都很稳定，颅神经通常不受累。部分病人虽然存在基因突变，但无肌无力和肌萎缩，仅有弓形足或神经传导速度减慢，有的甚至完全无临床症状。CMTII型(轴索型)：lateonset，muscleatrophyoccuratadult，clinicalfeaturesarethesameasCMTI型.Butlighterthanit；CSF:Proteinisnormal。,.,47,4.Labstudies(1)检查神经传导速度(NerveconductionvelocityNCV)对分型至关重要。CMT1型运动NCV从正常的50米/秒减慢为38米/秒以下，CMT2型NCV接近正常。(2)X连锁显性遗传患者脑干听觉诱发电位和视觉诱发电位异常，躯体感觉诱发电位的中枢和周围传导速度减慢。,.,48,(3)MuscleBiopsy:neurogenicatrophy;(4).NerveBiopsy:CMTI型的周围神经改变主要是脱髓鞘和雪旺氏细胞增生形成“onionbulb”；CMTII型主要是轴突变性。神经活检还可排除其他遗传性神经病。(5)cerebrospinalfluid:normal，少数病例蛋白含量增高。,.,49,5.Diagnosisanddifferentialdiagnosis临床诊断依据：(1).儿童期或青春期出现缓慢进展的对称性双下肢无力；(2).Storkleg，footd