{"id":88137,"date":"2018-03-10T00:13:03","date_gmt":"2018-03-10T00:13:03","guid":{"rendered":"https:\/\/www.deberes.net\/tesis\/sin-categoria\/diagnostico-citogenetico-prenatal-en-cataluna-durante-10-anos1986-1995\/"},"modified":"2018-03-10T00:13:03","modified_gmt":"2018-03-10T00:13:03","slug":"diagnostico-citogenetico-prenatal-en-cataluna-durante-10-anos1986-1995","status":"publish","type":"post","link":"https:\/\/www.deberes.net\/tesis\/ciencias-de-la-vida\/diagnostico-citogenetico-prenatal-en-cataluna-durante-10-anos1986-1995\/","title":{"rendered":"Diagnostico citogenetico prenatal en catalu\u00f1a durante 10 a\u00f1os:1986-1995"},"content":{"rendered":"<h2>Tesis doctoral de <strong> Nuria Clusellas Casals <\/strong><\/h2>\n<p>En este trabajo se recoge y analiza la informacion sobre el diagnostico prenatal(dp) de cromosomopatias en catalu\u00f1a realizado en diferentes laboratorios durante 10 a\u00f1os, 1986-1995. En total sehan recogido 46469 dp, de los cuales 7171 fueron realizados en muestras de vellosidades coriales y 39298 en muestras de liquido amniotico.  durante este periodo se analizan las variaciones en la practica del dp, teniendo en cuenta: la tasa anual de utilizacion global y seg\u00fan edad materna, indicaciones para el estudio citogenetico, tipo de muestra utilizada, referencia de las gestantes y tasa anual de anomalias.  en total se han diagnosticado 1043 anomalias, analizando su frecuencia seg\u00fan diferentes parametros: tipo de muestra, indicacion para el estudio, semanas de gestacion y edad materna.  a partir de los resultados obtenidos, se ha aplicado un modelo estadistico de regresion logistica que ha permitido relacionar todos los factores disponibles que pueden influir en la deteccion de anomalias cromosomicas y establecer un modelo predictivo.  la anomalias cromosomicas diagnosticadas se analizan seg\u00fan: el tipo de anomalia, frecuencia, indicacion principal y razon sexual. Las anomalias mas frecuentes son: la trisomia 21(34,13%) y anomalias estructurales equilibradas(23,78%).  las anomalias estructurales familiares se analizan valorando el riesgo de segregaci\u00f3n desequilibrada seg\u00fan el tipo de anomalia, sexo del progenitor portador, motivo de diagnostico de la reorganizaci\u00f3n y tama\u00f1o del segmento implicado en el desequilibrio.  se ha realizado el seguimiento del 38% de los casos con anomalias cromos\u00f3micas hasta el momento del nacimiento, la interrupcion del embarazo o perdida espontanea, incidiendo en el seguimiento de los casos con anomalias estructurales equilibradas y cromosomas marcadores de novo, para poder establecer el riesgo de anomalia congenita.<\/p>\n<p>&nbsp;<\/p>\n<h3>Datos acad\u00e9micos de la tesis doctoral \u00ab<strong>Diagnostico citogenetico prenatal en catalu\u00f1a durante 10 a\u00f1os:1986-1995<\/strong>\u00ab<\/h3>\n<ul>\n<li><strong>T\u00edtulo de la tesis:<\/strong>\u00a0 Diagnostico citogenetico prenatal en catalu\u00f1a durante 10 a\u00f1os:1986-1995 <\/li>\n<li><strong>Autor:<\/strong>\u00a0 Nuria Clusellas Casals <\/li>\n<li><strong>Universidad:<\/strong>\u00a0 Aut\u00f3noma de barcelona<\/li>\n<li><strong>Fecha de lectura de la tesis:<\/strong>\u00a0 19\/12\/2000<\/li>\n<\/ul>\n<p>&nbsp;<\/p>\n<h3>Direcci\u00f3n y tribunal<\/h3>\n<ul>\n<li><strong>Director de la tesis<\/strong>\n<ul>\n<li>Mar\u00eda  Dolors Coll Sandiumenge<\/li>\n<\/ul>\n<\/li>\n<li><strong>Tribunal<\/strong>\n<ul>\n<li>Presidente del tribunal: jos\u00e9 Egozcue cuixart <\/li>\n<li>joaquina Gabarron llamas (vocal)<\/li>\n<li>cristina Templado messeguer (vocal)<\/li>\n<li>anna Soler casas (vocal)<\/li>\n<\/ul>\n<\/li>\n<\/ul>\n<p>&nbsp;<\/p>\n","protected":false},"excerpt":{"rendered":"<p>Tesis doctoral de Nuria Clusellas Casals En este trabajo se recoge y analiza la informacion sobre el diagnostico prenatal(dp) de [&hellip;]<\/p>\n","protected":false},"author":1,"featured_media":0,"comment_status":"open","ping_status":"open","sticky":false,"template":"","format":"standard","meta":{"site-sidebar-layout":"default","site-content-layout":"","ast-site-content-layout":"","site-content-style":"default","site-sidebar-style":"default","ast-global-header-display":"","ast-banner-title-visibility":"","ast-main-header-display":"","ast-hfb-above-header-display":"","ast-hfb-below-header-display":"","ast-hfb-mobile-header-display":"","site-post-title":"","ast-breadcrumbs-content":"","ast-featured-img":"","footer-sml-layout":"","theme-transparent-header-meta":"","adv-header-id-meta":"","stick-header-meta":"","header-above-stick-meta":"","header-main-stick-meta":"","header-below-stick-meta":"","astra-migrate-meta-layouts":"default","ast-page-background-enabled":"default","ast-page-background-meta":{"desktop":{"background-color":"var(--ast-global-color-4)","background-image":"","background-repeat":"repeat","background-position":"center center","background-size":"auto","background-attachment":"scroll","background-type":"","background-media":"","overlay-type":"","overlay-color":"","overlay-gradient":""},"tablet":{"background-color":"","background-image":"","background-repeat":"repeat","background-position":"center center","background-size":"auto","background-attachment":"scroll","background-type":"","background-media":"","overlay-type":"","overlay-color":"","overlay-gradient":""},"mobile":{"background-color":"","background-image":"","background-repeat":"repeat","background-position":"center center","background-size":"auto","background-attachment":"scroll","background-type":"","background-media":"","overlay-type":"","overlay-color":"","overlay-gradient":""}},"ast-content-background-meta":{"desktop":{"background-color":"var(--ast-global-color-5)","background-image":"","background-repeat":"repeat","background-position":"center center","background-size":"auto","background-attachment":"scroll","background-type":"","background-media":"","overlay-type":"","overlay-color":"","overlay-gradient":""},"tablet":{"background-color":"var(--ast-global-color-5)","background-image":"","background-repeat":"repeat","background-position":"center center","background-size":"auto","background-attachment":"scroll","background-type":"","background-media":"","overlay-type":"","overlay-color":"","overlay-gradient":""},"mobile":{"background-color":"var(--ast-global-color-5)","background-image":"","background-repeat":"repeat","background-position":"center center","background-size":"auto","background-attachment":"scroll","background-type":"","background-media":"","overlay-type":"","overlay-color":"","overlay-gradient":""}},"footnotes":""},"categories":[849,212,35,9224,2820],"tags":[34309,184077,184076,1331,29122,159293],"class_list":["post-88137","post","type-post","status-publish","format-standard","hentry","category-biologia-celular","category-biologia-humana","category-ciencias-de-la-vida","category-citogenetica","category-genetica-humana","tag-anna-soler-casas","tag-cristina-templado-messeguer","tag-joaquina-gabarron-llamas","tag-jose-egozcue-cuixart","tag-maria-dolors-coll-sandiumenge","tag-nuria-clusellas-casals"],"_links":{"self":[{"href":"https:\/\/www.deberes.net\/tesis\/wp-json\/wp\/v2\/posts\/88137","targetHints":{"allow":["GET"]}}],"collection":[{"href":"https:\/\/www.deberes.net\/tesis\/wp-json\/wp\/v2\/posts"}],"about":[{"href":"https:\/\/www.deberes.net\/tesis\/wp-json\/wp\/v2\/types\/post"}],"author":[{"embeddable":true,"href":"https:\/\/www.deberes.net\/tesis\/wp-json\/wp\/v2\/users\/1"}],"replies":[{"embeddable":true,"href":"https:\/\/www.deberes.net\/tesis\/wp-json\/wp\/v2\/comments?post=88137"}],"version-history":[{"count":0,"href":"https:\/\/www.deberes.net\/tesis\/wp-json\/wp\/v2\/posts\/88137\/revisions"}],"wp:attachment":[{"href":"https:\/\/www.deberes.net\/tesis\/wp-json\/wp\/v2\/media?parent=88137"}],"wp:term":[{"taxonomy":"category","embeddable":true,"href":"https:\/\/www.deberes.net\/tesis\/wp-json\/wp\/v2\/categories?post=88137"},{"taxonomy":"post_tag","embeddable":true,"href":"https:\/\/www.deberes.net\/tesis\/wp-json\/wp\/v2\/tags?post=88137"}],"curies":[{"name":"wp","href":"https:\/\/api.w.org\/{rel}","templated":true}]}}