{"id":1005,"date":"2021-01-07T20:55:53","date_gmt":"2021-01-07T20:55:53","guid":{"rendered":"https:\/\/pitema.lt\/?page_id=1005"},"modified":"2021-01-07T20:56:59","modified_gmt":"2021-01-07T20:56:59","slug":"kaciu-genines-ligos","status":"publish","type":"page","link":"https:\/\/pitema.lt\/en\/kaciu-genines-ligos\/","title":{"rendered":"Ka\u010di\u0173 genin\u0117s ligos"},"content":{"rendered":"<div data-elementor-type=\"wp-page\" data-elementor-id=\"1005\" class=\"elementor elementor-1005\" wpc-filter-elementor-widget=\"1\" data-elementor-post-type=\"page\">\n\t\t\t\t\t\t<section class=\"elementor-section elementor-top-section elementor-element elementor-element-93569d0 elementor-section-boxed elementor-section-height-default elementor-section-height-default\" data-id=\"93569d0\" data-element_type=\"section\" data-e-type=\"section\">\n\t\t\t\t\t\t<div class=\"elementor-container elementor-column-gap-default\">\n\t\t\t\t\t<div class=\"elementor-column elementor-col-100 elementor-top-column elementor-element elementor-element-8fc8d00\" data-id=\"8fc8d00\" data-element_type=\"column\" data-e-type=\"column\">\n\t\t\t<div class=\"elementor-widget-wrap elementor-element-populated\">\n\t\t\t\t\t\t<div class=\"elementor-element elementor-element-94a7fd1 elementor-vertical-align-top elementor-widget elementor-widget-image-box\" data-id=\"94a7fd1\" data-element_type=\"widget\" data-e-type=\"widget\" data-widget_type=\"image-box.default\">\n\t\t\t\t<div class=\"elementor-widget-container\">\n\t\t\t\t\t<div class=\"elementor-image-box-wrapper\"><div class=\"elementor-image-box-content\"><h3 class=\"elementor-image-box-title\">KA\u010cI\u0172 CHROMOSOMIN\u0116S IR GENIN\u0116S LIGOS BEI YDOS<\/h3><p class=\"elementor-image-box-description\">Paveldimi susirgimai \u2013 tai morfologiniai, funkciniai ir biocheminiai pakitimai atsirad\u0119 d\u0117l poky\u010di\u0173 genetin\u0117je informacijoje. Paveldima patologija gali pasireik\u0161ti \u012fvairiomis organ\u0173 ir audini\u0173 anomalijomis, abortais, vislumo suma\u017e\u0117jimu, \u012fvairiais funkciniais negalavimais arba med\u017eiag\u0173 apykaitos ligomis.\n\nVeterinarin\u0117je patogenetikoje skiriamos dvi susirgim\u0173 grup\u0117s :\n\n   chromosomin\u0117s ligos\n   genin\u0117s ligos\nGyvuli\u0173 chromosomin\u0117s ligos ir ydos da\u017eniausiai sukelia \u012fvairius reprodukcijos sutrikimus. \u017denkl\u016bs gamet\u0173 genetiniai defektai, ypa\u010d chromosom\u0173 skai\u010diaus pakitimai ir daugybin\u0117s aberacijos, s\u0105lygoja nevaisingum\u0105. Tokiu atveju vyksta prezigotin\u0117 selekcija ir sutrinka apvaisinimo procesas. Ma\u017ei gamet\u0173 genetiniai defektai s\u0105lygoja anomalijas, abortus, lytini\u0173 organ\u0173 ir lytinio ciklo sutrikimus.\n\nGyvuli\u0173 genin\u0117s ligos  sukelia ne tik \u012fvairius apsigimimus bei reprodukcijos sutrikimus, bet ir daugyb\u0119 \u012fvairi\u0173 paveldim\u0173 lig\u0173 i\u0161 kuri\u0173 daugelis yra letalios.\n\nDominantin\u0117s paveldimos ligos ir ydos \u2013 visada pasirei\u0161kia\nRecesyvin\u0117s paveldimos ligos ir ydos \u2013 pasirei\u0161kia tik tada, jei individas turi dvi geno kopijas. Jei turi vien\u0105 pakitusio geno kopij\u0105 toks individas bus pakitusio geno ne\u0161iotojas, kur\u012f galima identifikuoti tik molekuliniaias metodais i\u0161tyrus jo genom\u0105.\nBeuodegyst\u0117\nRy\u0161kus nugarkaulio sutrup\u0117jimas.\nTai autosominis ne visi\u0161kai dominantinis paveld\u0117jimas su kintamu ekspresyvumu.\nGenas M. Kat\u0117s su gen\u0173 kombinacija MM \u017e\u016bsta ankstyvoje embrion\u0173 stadijoje.\nGali b\u016bti paveiktas dubuo ar stuburo slanksteliai. Silpnos kojos ir p\u016bsl\u0117.\nManx, Japonijos bobtail ir Cymric veisli\u0173 kat\u0117ms\nSiamo kat\u0117ms mutacija pasirei\u0161kia uodegos u\u017esilenkimu.\n1 2\n\n \n\nPiruvato kinaz\u0117s tr\u016bkumas\nTai autosomin\u0117 recesyvin\u0117 liga\nAbessinier, somali veisl\u0117se\nRaudoniesiems kraujo k\u016bneliams tr\u016bksta piruvato kinaz\u0117s. Eritrocit\u0173 i\u0161gyvenimo laikotarpis sutrump\u0117ja. Suma\u017e\u0117ja j\u0173 skai\u010dius.\nPo keli\u0173 m\u0117nesi\u0173 pasirei\u0161kia anemijos simptonai arba kat\u0117s gai\u0161ta d\u0117l neai\u0161ki\u0173 prie\u017eas\u010di\u0173.\nPolicistiniai inkstai\nAutosomin\u0117 dominantin\u0117 pers\u0173, Egzot\u0173 trumpaplauki\u0173 ir kit\u0173 i\u0161vestini\u0173 veisli\u0173 liga\nPolicistiniai inkstai i\u0161sivysto vieno mutacinio geno d\u0117ka.\nHomozigotai \u017e\u016bsta embriono stadijoje arba inkst\u0173 nepakankamumas i\u0161sivysto ankstyvame am\u017eiuje.\nNormalus inkstas; \u0161e\u0161i\u0173 savai\u010di\u0173 am\u017eiaus.\n\n3\n\n \n\nKat\u0117s policistinis inkstas\n\n 4\n\nSuaugusios kat\u0117s paskutin\u0117s stadijos policistinis inkstas.\n\n5\n\n \n\nOsteochondrodisplazija\n 6 7\n\nAutosomin\u0117 dominantin\u0117 \u0160kot\u0173 veisl\u0117s ka\u010di\u0173 liga.\nDefektinis genas, d\u0117l kurio \u201cu\u017esilenkia\u201d ausys nulemia artrito i\u0161sivystym\u0105.\n\u0160ios veisl\u0117s kat\u0117ms su normaliomis ausimis liga nepasirei\u0161kia.\nKa\u010di\u0173 kurtumas\n 8\n\nVis\u0173 veisli\u0173 visi\u0161kai balto kailio m\u0117lynaki\u0173 ka\u010di\u0173, bei Meino Me\u0161k\u0117n\u0173 veisl\u0117s defektas.\nKat\u0117s, kuri\u0173 akys skirting\u0173 spalv\u0173 re\u010diau b\u016bna kur\u010dios, arba negirdi tik viena (m\u0117lynos akies) puse.\nKurtum\u0105 \u012ftakoja dominantinis W genas.\n60% baltakaili\u0173 ilgaplauki\u0173 ka\u010di\u0173 yra kur\u010dios.\n      6.Achondroplazija, pseudoplazija, hipochondroplazija\n\n9\n\n \n\nAutosomin\u0117 dominuojanti, pusiau l\u0117tali.\nAchondroplazin\u012f \u017eema\u016bgi\u0161kum\u0105 rodo trumpos kojos ir padid\u0117jusi galva; pseudoachondroplazij\u0105rodo trumpos gal\u016bn\u0117s ir normali galva.\nSu Munhkin mutacija susijusi yra lordoz\u0117 (stuburo i\u0161krypimas \u012f priek\u012f) ir pectus (i\u0161plat\u0117jusi \u0161onkauli\u0173 riba).\nPaveld\u0117jus 2 kopijas genas yra mirtinas.\nBeplauki\u0161kumas (hypotrichosis)\nEgzistuoja recesyvin\u0117 ir dominantin\u0117 formos.\nSfinks\u0173, Donskoy, kai kurios Reks\u0173 veisl\u0117s.\nBeplauk\u0117s paprastai turi normali\u0105 k\u016bno dang\u0105, kurios gali netekti senstant.?\nJautrios ekstremalioms oro ar laikymo s\u0105lygoms.\n  1112\n\n \n\nPlok\u0161\u010diakr\u016btinini\u0173 ka\u010diuk\u0173 sindromas\nL\u0117talin\u0117\/\u017ealojanti, recesyvin\u0117.\nB\u016bdinga bet kuriai veislei, ta\u010diau da\u017eniau pasitaiko Birmos.\nKr\u016btin\u0117 \u012fgaubta. Ka\u010diukai turi kv\u0117pavimo problem\u0173, i\u0161sek\u0119 ir pasi\u017eymi ne\u016b\u017eaugoms b\u016bdingu augimu.\nSutrikdyti vidaus organai.\nSunk\u016bs atvejai baigiasi mirtimi.\nKeturios ausys\nRecesyvin\u0117\nKat\u0117 turi ma\u017e\u0105, papildom\u0105 aus\u0173 por\u0105\nGali b\u016bti ma\u017eos akys, \u017eandikaulis nesuvertas. Ypatingos formos galva ir pastebimas mieguistumas\/apatija.\n\n13\n\n \n\nPolidaktilija\nMonogenin\u0117 dominuojanti\nGali b\u016bti: padid\u0117jusios letenos, letenos be nyk\u0161\u010di\u0173, papildomi pir\u0161tai.\nThumb-cat rudimentin\u0117 atauga pavirtusi nyk\u0161\u010diu\nTwisty  \u2013 vingiuotos kat\u0117s sindromas: \u201cm\u0117sainio p\u0117dos\u201d forma \u2013 papildomi pir\u0161tai suaug\u0119 ir n\u0117ra atskir\u0173 nyk\u0161\u010di\u0173\n14<\/p><\/div><\/div>\t\t\t\t<\/div>\n\t\t\t\t<\/div>\n\t\t\t\t\t<\/div>\n\t\t<\/div>\n\t\t\t\t\t<\/div>\n\t\t<\/section>\n\t\t\t\t<\/div>","protected":false},"excerpt":{"rendered":"<p>KA\u010cI\u0172 CHROMOSOMIN\u0116S IR GENIN\u0116S LIGOS BEI YDOS Paveldimi susirgimai \u2013 tai morfologiniai, funkciniai ir biocheminiai pakitimai atsirad\u0119 d\u0117l poky\u010di\u0173 genetin\u0117je informacijoje. Paveldima patologija gali pasireik\u0161ti \u012fvairiomis organ\u0173 ir audini\u0173 anomalijomis, abortais, vislumo suma\u017e\u0117jimu, \u012fvairiais funkciniais negalavimais arba med\u017eiag\u0173 apykaitos ligomis. Veterinarin\u0117je patogenetikoje skiriamos dvi susirgim\u0173 grup\u0117s : chromosomin\u0117s ligos genin\u0117s ligos Gyvuli\u0173 chromosomin\u0117s ligos ir&hellip;<\/p>","protected":false},"author":1,"featured_media":0,"parent":0,"menu_order":0,"comment_status":"closed","ping_status":"closed","template":"","meta":{"footnotes":""},"class_list":["post-1005","page","type-page","status-publish","hentry"],"yoast_head":"<!-- This site is optimized with the Yoast SEO plugin v28.2 - https:\/\/yoast.com\/product\/yoast-seo-wordpress\/ -->\n<title>Ka\u010di\u0173 genin\u0117s ligos - Pitema.lt<\/title>\n<meta name=\"robots\" content=\"index, follow, max-snippet:-1, max-image-preview:large, max-video-preview:-1\" \/>\n<link rel=\"canonical\" href=\"https:\/\/pitema.lt\/en\/kaciu-genines-ligos\/\" \/>\n<meta property=\"og:locale\" content=\"en_US\" \/>\n<meta property=\"og:type\" content=\"article\" \/>\n<meta property=\"og:title\" content=\"Ka\u010di\u0173 genin\u0117s ligos - Pitema.lt\" \/>\n<meta property=\"og:description\" content=\"KA\u010cI\u0172 CHROMOSOMIN\u0116S IR GENIN\u0116S LIGOS BEI YDOS Paveldimi susirgimai \u2013 tai morfologiniai, funkciniai ir biocheminiai pakitimai atsirad\u0119 d\u0117l poky\u010di\u0173 genetin\u0117je informacijoje. 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Paveldima patologija gali pasireik\u0161ti \u012fvairiomis organ\u0173 ir audini\u0173 anomalijomis, abortais, vislumo suma\u017e\u0117jimu, \u012fvairiais funkciniais negalavimais arba med\u017eiag\u0173 apykaitos ligomis. 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