{"id":14181,"date":"2016-01-25T12:34:17","date_gmt":"2016-01-25T12:34:17","guid":{"rendered":"http:\/\/www.asperbio.com\/?page_id=14181"},"modified":"2026-05-08T14:40:45","modified_gmt":"2026-05-08T11:40:45","slug":"asper-otogenetics-testid","status":"publish","type":"page","link":"https:\/\/www.asperbio.com\/et\/asper-otogenetics-testid\/","title":{"rendered":"Asper Otogenetics testid"},"content":{"rendered":"

Asper Otogenetics\u00a0<\/span><\/h1>\n
\n

Alporti s\u00fcndroom<\/a><\/strong>
\n Aminogl\u00fckosiididest tingitud kurtus<\/a><\/strong>
\n Branchio-oto-renaalne s\u00fcndroom<\/a><\/strong>
\n Jervelli ja Lange-Nielsoni s\u00fcndroom<\/a><\/strong>
\n Mitokondriaalsed haigused<\/a><\/strong>
\n Pendredi s\u00fcndroom<\/a><\/strong>
\n Refsumi t\u00f5bi ja Zellwegeri s\u00fcndroom<\/a><\/strong>
\n Sensorineuraalne kuulmislangus<\/a> <\/strong>
\n Stickleri s\u00fcndroom<\/a><\/strong>
\n Treacher-Collinsi s\u00fcndroom<\/a><\/strong>
\n Usheri s\u00fcndroom<\/a><\/strong>
\n Waardenburgi s\u00fcndroom<\/a><\/strong>
\n Eksoomi sekveneerimine<\/strong><\/a><\/h4>\n<\/div>\n

Asper Otogenetics portfell sisaldab erinevaid geeniteste nii s\u00fcndroomsete kui mitte-s\u00fcndroomsete kuulmislanguse ja kurtuse p\u00e4rilike vormide m\u00e4\u00e4ramiseks.\u00a0Kuna selle haigustegrupi puhul on diagnoosi kinnitamine keeruline suure geneetilise varieeruvuse ja fenot\u00fc\u00fcpide kattumise t\u00f5ttu, oleme v\u00e4ljat\u00f6\u00f6tanud multigeensed uuringupaneelid kuulmislanguse geneetiliste p\u00f5hjuste tuvastamiseks.\u00a0Pakume ka \u00fche-geeni uuringuid GJB2<\/em> geeni-seoseliste haiguste, Pendred s\u00fcndroomi ja teiste s\u00fcndroomsete kuulmislanguse vormide m\u00e4\u00e4ramiseks. P\u00e4riliku kuulmislanguse ja kurtuse vormide\u00a0diferentsiaaldiagnostika\u00a0v\u00f5imaldab pakkuda t\u00e4pset geneetilist n\u00f5ustamist ja kordusriskide m\u00e4\u00e4ramist, tagades\u00a0personaalse l\u00e4henemise nii patsientidele kui\u00a0nende pereliikmetele.<\/p>\n

Juhul, kui \u00a0meie loetelus soovitud anal\u00fc\u00fcsi ei leidnud v\u00f5i soovite erinevaid paneele kombineerida, andke palun saatelehel soovist teada. Vahel v\u00f5ib otsitav anal\u00fc\u00fcs olla ka teise portfelli nimekirjas<\/span>.<\/p>\n

Geenitestide \u00a0tegemiseks kasutame erinevaid molekulaargeneetilisi meetodeid nagu DNA sekveneerimine, sealhulgas Sanger sekveneerimine ja teise p\u00f5lvkonna sekveneerimine (Next Generation Sequencing<\/em>, NGS), Real-Time PCR, DNA l\u00f5ikude deletsioonide\/duplikatsioonide anal\u00fc\u00fcsi (MLPA meetod), DNA fragmentanal\u00fc\u00fcs ja DNA restriktsioonanal\u00fc\u00fcs (RFLP).\u00a0NGS-tehnoloogia v\u00f5imaldab operatiivseid\u00a0ja personaalseid geenitestide erilahendusi vastavalt patsiendi spetsiifilistele vajadustele.<\/p>","protected":false},"excerpt":{"rendered":"

Asper Otogenetics\u00a0 Alporti s\u00fcndroom Aminogl\u00fckosiididest tingitud kurtus Branchio-oto-renaalne s\u00fcndroom Jervelli ja Lange-Nielsoni s\u00fcndroom Mitokondriaalsed haigused Pendredi s\u00fcndroom Refsumi t\u00f5bi ja Zellwegeri s\u00fcndroom Sensorineuraalne kuulmislangus Stickleri s\u00fcndroom Treacher-Collinsi s\u00fcndroom Usheri s\u00fcndroom Waardenburgi s\u00fcndroom Eksoomi sekveneerimine Asper Otogenetics portfell sisaldab erinevaid geeniteste nii s\u00fcndroomsete kui mitte-s\u00fcndroomsete kuulmislanguse ja kurtuse p\u00e4rilike vormide m\u00e4\u00e4ramiseks.\u00a0Kuna selle haigustegrupi puhul on diagnoosi […]<\/p>\n","protected":false},"author":2,"featured_media":0,"parent":0,"menu_order":14,"comment_status":"closed","ping_status":"closed","template":"","meta":{"_monsterinsights_skip_tracking":false,"_monsterinsights_sitenote_active":false,"_monsterinsights_sitenote_note":"","_monsterinsights_sitenote_category":0,"footnotes":""},"class_list":["post-14181","page","type-page","status-publish","hentry"],"aioseo_notices":[],"_links":{"self":[{"href":"https:\/\/www.asperbio.com\/et\/wp-json\/wp\/v2\/pages\/14181","targetHints":{"allow":["GET"]}}],"collection":[{"href":"https:\/\/www.asperbio.com\/et\/wp-json\/wp\/v2\/pages"}],"about":[{"href":"https:\/\/www.asperbio.com\/et\/wp-json\/wp\/v2\/types\/page"}],"author":[{"embeddable":true,"href":"https:\/\/www.asperbio.com\/et\/wp-json\/wp\/v2\/users\/2"}],"replies":[{"embeddable":true,"href":"https:\/\/www.asperbio.com\/et\/wp-json\/wp\/v2\/comments?post=14181"}],"version-history":[{"count":3,"href":"https:\/\/www.asperbio.com\/et\/wp-json\/wp\/v2\/pages\/14181\/revisions"}],"predecessor-version":[{"id":29657,"href":"https:\/\/www.asperbio.com\/et\/wp-json\/wp\/v2\/pages\/14181\/revisions\/29657"}],"wp:attachment":[{"href":"https:\/\/www.asperbio.com\/et\/wp-json\/wp\/v2\/media?parent=14181"}],"curies":[{"name":"wp","href":"https:\/\/api.w.org\/{rel}","templated":true}]}}