Molecular diagnosis of Huntington disease in Portugal : implications for genetic counselling and clinical practice

dc.contributor.authorCosta, Maria do Carmo
dc.contributor.authorMagalhães, Paula
dc.contributor.authorFerreirinha, Fátima
dc.contributor.authorGuimarães, Laura
dc.contributor.authorJanuário, Cristina
dc.contributor.authorGaspar, Isabel
dc.contributor.authorLoureiro, Leal
dc.contributor.authorVale, José
dc.contributor.authorGarrett, Carolina
dc.contributor.authorRegateiro, Fernando
dc.contributor.authorMagalhães, Marina
dc.contributor.authorSousa, Alda
dc.contributor.authorMaciel, P.
dc.contributor.authorSequeiros, Jorge
dc.date.accessioned2006-11-06T14:30:33Z
dc.date.available2006-11-06T14:30:33Z
dc.date.issued2003-11
dc.description.abstractHuntington disease (HD) is a eurodegenerative, autosomal dominant disorder of late-onset, caused by the expansion of a CAG repeat in the coding region of the gene. Ours is the reference laboratory for genetic testing in HD, in Portugal, since 1998; 90.1% of all 158 families known were identified for the first time, including patients with unusual presentation or without family history. A total of 338 genetic tests were performed: 234 for diagnosis, 96 for presymptomatic and four for prenatal testing (four were done for family studies). Most referring physicians were neurologists (90.6%); 82.8% of all clinical diagnosis were confirmed, while 83.1% of those sent for exclusion were in fact excluded. In presymptomatic testing, an excess of female subjects (59.4%) was again verified; 37.5% of the consultands were found to be carriers. None of the foetuses, in four prenatal tests, were mutation carriers. One juvenile case was inherited from her mother. Our patient population is very similar to others described so far, namely in terms of mean age at onset and (CAG)n distribution, except perhaps for a higher frequency of large normal (class 2) alleles (3.7%). We also identify cases posing particular problems for genetic counselling, such as, ‘homozygosity’ that can pose a serious ethical dilemma, carriers of large normal alleles, and ‘homoallelism’ for a normal gene, which will demand further procedures and may delay results in presymptomatic and prenatal testing.eng
dc.distributioninternationalpor
dc.identifier.citation"European journal of human genetics". ISSN 1018-4813. 11:11(Nov.2003) 872-878.eng
dc.identifier.doi10.1038/sj.ejhg.5201055por
dc.identifier.issn1018-4813eng
dc.identifier.pmid14571273por
dc.identifier.urihttps://hdl.handle.net/1822/5745
dc.language.isoengeng
dc.peerreviewedyespor
dc.publisherNature Publishing Grouppor
dc.rightsopenAccesseng
dc.subjectPolyglutamine disorderseng
dc.subjectCommunity geneticseng
dc.subjectGenetic testingeng
dc.subjectHomozygosityeng
dc.subjectHomoallelismeng
dc.subjectIntermediate alleleseng
dc.subjectEthical dilemmaeng
dc.subject.wosScience & Technologypor
dc.titleMolecular diagnosis of Huntington disease in Portugal : implications for genetic counselling and clinical practiceeng
dc.typearticlepor
dspace.entity.typePublicationen
oaire.citationEndPage878por
oaire.citationIssue11por
oaire.citationStartPage872por
oaire.citationVolume11por
sdum.journalEuropean Journal of Human Geneticspor
sdum.number11eng
sdum.pagination872–878eng
sdum.publicationstatuspublishedeng
sdum.volume11eng

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