Genomics and Perinatal Care基因組學與圍產(chǎn)期保健

Genomics and Perinatal Care基因組學與圍產(chǎn)期保健

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時間:2019-08-08

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1、ReviewarticleGenomicMedicineW.GregoryFeero,M.D.,Ph.D.,andAlanE.Guttmacher,M.D.,EditorsGenomicsandPerinatalCareJoannBodurtha,M.D.,M.P.H.,andJeromeF.Strauss,III,M.D.,Ph.D.FromtheMcKusick–NathansInstituteofmongbothprospectiveparentsandprovidersofmedicalcare,GeneticMedicine,JohnsHopkinsMedic

2、algeneticandsocialconcernspeakduringtheperinatalperiod.AdvancesinInstitutions,Baltimore(J.B.);andtheDe-ApartmentofObstetricsandGynecology,genomicsandassistedreproductivetechnologyhavecreatednewopportuni-VirginiaCommonwealthUniversity,Rich-tiestodetectgeneticdisordersandsusceptibilitiesat

3、multipletimesduringperina-mond(J.F.S.).Addressreprintrequeststotalcareandthusarerelevanttotheseconcerns.Emergingtherapiesforsingle-geneDr.StraussattheDepartmentofObstet-ricsandGynecology,VirginiaCommon-disordersmayreshapethesediscussions.wealthUniversity,1101E.MarshallSt.,Practitionerswo

4、rkingwithpersonswishingtobeparentsareencouragedtoinquireRichmond,VA23298,oratjfstrauss@abouttheirgeneticbackgroundsandfamilyhistories,tocounselthemabouttestsforvcu.edu.disease-carrierstatusthatarebasedonknownpopulation-specificrisks,1andtoreferNEnglJMed2012;366:64-73.them,whenappropriate

5、,tospecialistsinhigh-riskpregnancyandgenetics.Nonethe-Copyright?2012MassachusettsMedicalSociety.less,therearemajordifferencesacrosstheworldintheadoptionandimplementationofgeneticeducationandscreeningpracticesbyproviders,womenandtheirpartners,andhealthpaymentsystems.2,3Suchdifferencesaret

6、obeexpectedbecauseaccesstohealthcare,alongwiththeavailabilityofgeneticcounselingandtesting,varies.Eveninthebest-casescenario,patients,practitioners,andpolicymakersfacecom-plicatedchoiceswhenselectingwhichgenomictechniquestousebroadlyorindividu-allyinassessingriskandindetermininghowlabora

7、toryfindingsshouldinformdeci-sionmakingastheoptionsforgenetictestingexpand.4Forexample,itisnotalwayspossibletopredictaprioritheseverityofaclinicalconditiononthebasisofageno-type.Alaboratoryresultmaybeflawless,buttheidentifiedgeneticvariationmaynotbeknowntocauseadisease(i.

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