Diagn\u00f3stico gen\u00e9tico preimplantacional para enfermedades monog\u00e9nicas<\/title>\n <style>\n body{ \n margin:0; \n font-family: Georgia, 'Times New Roman', serif; \n background:#f4f6f9; \n color:#222; \n }\n .blog-container{ \n max-width:900px; \n margin:80px auto; \n padding:0 20px; \n }\n .blog-container h2{ \n font-size:34px; \n margin-bottom:40px; \n font-weight:600; \n text-align:center; \n position:relative; \n line-height: 1.2;\n }\n .blog-container h2::after{ \n content:\"\"; \n width:80px; \n height:3px; \n background:#1f3c88; \n display:block; \n margin:15px auto 0; \n border-radius:2px; \n }\n .blog-container p, .blog-container ul{ \n font-size:18px; \n line-height:1.9; \n text-align:justify; \n margin-bottom:25px; \n }\n .img-left{ \n float:left; \n width:320px; \n margin:10px 30px 20px 0; \n border-radius:12px; \n box-shadow:0 10px 30px rgba(0,0,0,0.12); \n }\n .img-right{ \n float:right; \n width:350px; \n margin:10px 0 20px 30px; \n border-radius:12px; \n box-shadow:0 10px 30px rgba(0,0,0,0.12); \n }\n .clear{ \n clear:both; \n }\n @media (max-width:768px){\n .blog-container{ margin:50px auto; }\n .blog-container h2{ font-size:28px; }\n .blog-container p, .blog-container ul{ font-size:16px; }\n .img-left, .img-right{ \n float:none; \n width:100%; \n margin:0 0 20px 0; \n }\n }\n <\/style>\n<\/head>\n<body>\n\n<section class=\"blog-container\">\n <h2>Diagn\u00f3stico gen\u00e9tico preimplantacional para enfermedades monog\u00e9nicas<\/h2>\n\n <p>\n El <strong>PGT-M<\/strong> (Preimplantation Genetic Testing for Monogenic Disorders) es una prueba que permite identificar si un embri\u00f3n es portador o est\u00e1 afectado por una enfermedad gen\u00e9tica causada por un solo gen. Su objetivo es ayudar a las familias con riesgo hereditario a tener un beb\u00e9 sano, evitando la transmisi\u00f3n de una condici\u00f3n gen\u00e9tica espec\u00edfica.\n <\/p>\n\n <img data-recalc-dims=\"1\" decoding=\"async\" loading=\"lazy\" src=\"https:\/\/i0.wp.com\/fertility.com.gt\/wp-content\/uploads\/2026\/05\/D758959-scaled.jpg?w=1020&ssl=1\" alt=\"PGT-M an\u00e1lisis gen\u00e9tico\" class=\"img-right\">\n\n <p>\n Este estudio se recomienda cuando uno o ambos miembros de la pareja tienen una enfermedad gen\u00e9tica conocida, mutaciones identificadas en estudios de portadores, antecedentes familiares de trastornos hereditarios graves o riesgo de transmitir condiciones autos\u00f3micas dominantes, recesivas o ligadas al cromosoma X.\n <\/p>\n\n <p>\n Antes de iniciar el ciclo de FIV, el centro en conjunto con el laboratorio de gen\u00e9tica dise\u00f1a un an\u00e1lisis personalizado para la familia, utilizando t\u00e9cnicas de secuenciaci\u00f3n y marcadores ligados al gen afectado.\n <\/p>\n\n <img data-recalc-dims=\"1\" decoding=\"async\" loading=\"lazy\" src=\"https:\/\/i0.wp.com\/fertility.com.gt\/wp-content\/uploads\/2026\/05\/D758945-scaled.jpg?w=1020&ssl=1\" alt=\"Biopsia de blastocisto\" class=\"img-left\">\n\n <p>\n Luego, se realiza la FIV y los embriones que alcanzan la etapa de blastocisto (d\u00eda 5-6), mediante un l\u00e1ser especial se realiza un orificio similar al que el embri\u00f3n har\u00e1 en el momento de eclosionar, disminuyendo la posibilidad de da\u00f1o. Posteriormente, se toma una peque\u00f1a muestra de c\u00e9lulas (5-10) del trofectodermo, que formar\u00e1 la placenta, sin afectar su capacidad de desarrollo.\n <\/p>\n\n <p>\n Esa muestra se env\u00eda a un laboratorio especializado que utiliza tecnolog\u00eda de secuenciaci\u00f3n de \u00faltima generaci\u00f3n para evaluar los cromosomas. Solo aquellos embriones con los 46 cromosomas contin\u00faan el an\u00e1lisis para detectar el gen mutado.\n <\/p>\n\n <img data-recalc-dims=\"1\" decoding=\"async\" loading=\"lazy\" src=\"https:\/\/i0.wp.com\/fertility.com.gt\/wp-content\/uploads\/2026\/05\/D758451-scaled.jpg?w=1020&ssl=1\" alt=\"Tecnolog\u00eda gen\u00e9tica avanzada\" class=\"img-right\">\n\n <p><strong>Con este estudio se determina si el embri\u00f3n est\u00e1:<\/strong><\/p>\n <ul>\n <li>Sano<\/li>\n <li>Portador (sin manifestar la enfermedad)<\/li>\n <li>Afectado<\/li>\n <\/ul>\n\n <p>\n Solo se transfieren los embriones libres de la enfermedad y, en algunos casos, seg\u00fan la condici\u00f3n y el consejo gen\u00e9tico, tambi\u00e9n pueden considerarse embriones portadores.\n <\/p>\n\n <p>\n El PGT-M es una herramienta poderosa para prevenir enfermedades hereditarias como fibrosis qu\u00edstica, distrofias musculares, anemia falciforme, enfermedades metab\u00f3licas y epilepsias gen\u00e9ticas, entre muchas otras.\n <\/p>\n\n <p>\n En <strong>Fertility Guatemala<\/strong> acompa\u00f1amos a cada familia desde el estudio inicial hasta la interpretaci\u00f3n detallada de resultados. Combinamos FIV avanzada, gen\u00e9tica de precisi\u00f3n y un apoyo humano cercano para ayudar a lograr un embarazo seguro y un beb\u00e9 sano en casa.\n <\/p>\n\n <div class=\"clear\"><\/div>\n<\/section>\n\n<\/body>\n<\/html>\n\n\n\n<p class=\"wp-block-paragraph\"><\/p>\n","protected":false},"excerpt":{"rendered":"<p>Diagn\u00f3stico gen\u00e9tico preimplantacional para enfermedades monog\u00e9nicas Diagn\u00f3stico gen\u00e9tico preimplantacional para enfermedades monog\u00e9nicas El PGT-M (Preimplantation Genetic Testing for Monogenic Disorders) es una prueba que permite identificar si un embri\u00f3n es portador o est\u00e1 afectado por una enfermedad gen\u00e9tica causada por un solo gen. Su objetivo es ayudar a las familias con riesgo hereditario a tener […]\n","protected":false},"author":1,"featured_media":0,"parent":0,"menu_order":0,"comment_status":"closed","ping_status":"closed","template":"","meta":{"nf_dc_page":"","om_disable_all_campaigns":false,"_monsterinsights_skip_tracking":false,"_monsterinsights_sitenote_active":false,"_monsterinsights_sitenote_note":"","_monsterinsights_sitenote_category":0,"_joinchat":[],"footnotes":""},"class_list":["post-746","page","type-page","status-publish","hentry"],"yoast_head":"\n<title>PGT-M - Fertility Guatemala<\/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:\/\/fertility.com.gt\/es\/pgt-m-2\/\" \/>\n<meta property=\"og:locale\" content=\"es_ES\" \/>\n<meta property=\"og:type\" content=\"article\" \/>\n<meta property=\"og:title\" content=\"PGT-M - Fertility Guatemala\" \/>\n<meta property=\"og:description\" content=\"Diagn\u00f3stico gen\u00e9tico preimplantacional para enfermedades monog\u00e9nicas Diagn\u00f3stico gen\u00e9tico preimplantacional para enfermedades monog\u00e9nicas El PGT-M (Preimplantation Genetic Testing for Monogenic Disorders) es una prueba que permite identificar si un embri\u00f3n es portador o est\u00e1 afectado por una enfermedad gen\u00e9tica causada por un solo gen. 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{"id":746,"date":"2026-01-22T13:42:08","date_gmt":"2026-01-22T13:42:08","guid":{"rendered":"https:\/\/fertility.com.gt\/?page_id=746"},"modified":"2026-05-01T15:12:12","modified_gmt":"2026-05-01T15:12:12","slug":"pgt-m-2","status":"publish","type":"page","link":"https:\/\/fertility.com.gt\/es\/pgt-m-2\/","title":{"rendered":"PGT-M"},"content":{"rendered":"\n\n\n\n \n \n Diagn\u00f3stico gen\u00e9tico preimplantacional para enfermedades monog\u00e9nicas<\/title>\n <style>\n body{ \n margin:0; \n font-family: Georgia, 'Times New Roman', serif; \n background:#f4f6f9; \n color:#222; \n }\n .blog-container{ \n max-width:900px; \n margin:80px auto; \n padding:0 20px; \n }\n .blog-container h2{ \n font-size:34px; \n margin-bottom:40px; \n font-weight:600; \n text-align:center; \n position:relative; \n line-height: 1.2;\n }\n .blog-container h2::after{ \n content:\"\"; \n width:80px; \n height:3px; \n background:#1f3c88; \n display:block; \n margin:15px auto 0; \n border-radius:2px; \n }\n .blog-container p, .blog-container ul{ \n font-size:18px; \n line-height:1.9; \n text-align:justify; \n margin-bottom:25px; \n }\n .img-left{ \n float:left; \n width:320px; \n margin:10px 30px 20px 0; \n border-radius:12px; \n box-shadow:0 10px 30px rgba(0,0,0,0.12); \n }\n .img-right{ \n float:right; \n width:350px; \n margin:10px 0 20px 30px; \n border-radius:12px; \n box-shadow:0 10px 30px rgba(0,0,0,0.12); \n }\n .clear{ \n clear:both; \n }\n @media (max-width:768px){\n .blog-container{ margin:50px auto; }\n .blog-container h2{ font-size:28px; }\n .blog-container p, .blog-container ul{ font-size:16px; }\n .img-left, .img-right{ \n float:none; \n width:100%; \n margin:0 0 20px 0; \n }\n }\n <\/style>\n<\/head>\n<body>\n\n<section class=\"blog-container\">\n <h2>Diagn\u00f3stico gen\u00e9tico preimplantacional para enfermedades monog\u00e9nicas<\/h2>\n\n <p>\n El <strong>PGT-M<\/strong> (Preimplantation Genetic Testing for Monogenic Disorders) es una prueba que permite identificar si un embri\u00f3n es portador o est\u00e1 afectado por una enfermedad gen\u00e9tica causada por un solo gen. Su objetivo es ayudar a las familias con riesgo hereditario a tener un beb\u00e9 sano, evitando la transmisi\u00f3n de una condici\u00f3n gen\u00e9tica espec\u00edfica.\n <\/p>\n\n <img data-recalc-dims=\"1\" decoding=\"async\" loading=\"lazy\" src=\"https:\/\/i0.wp.com\/fertility.com.gt\/wp-content\/uploads\/2026\/05\/D758959-scaled.jpg?w=1020&ssl=1\" alt=\"PGT-M an\u00e1lisis gen\u00e9tico\" class=\"img-right\">\n\n <p>\n Este estudio se recomienda cuando uno o ambos miembros de la pareja tienen una enfermedad gen\u00e9tica conocida, mutaciones identificadas en estudios de portadores, antecedentes familiares de trastornos hereditarios graves o riesgo de transmitir condiciones autos\u00f3micas dominantes, recesivas o ligadas al cromosoma X.\n <\/p>\n\n <p>\n Antes de iniciar el ciclo de FIV, el centro en conjunto con el laboratorio de gen\u00e9tica dise\u00f1a un an\u00e1lisis personalizado para la familia, utilizando t\u00e9cnicas de secuenciaci\u00f3n y marcadores ligados al gen afectado.\n <\/p>\n\n <img data-recalc-dims=\"1\" decoding=\"async\" loading=\"lazy\" src=\"https:\/\/i0.wp.com\/fertility.com.gt\/wp-content\/uploads\/2026\/05\/D758945-scaled.jpg?w=1020&ssl=1\" alt=\"Biopsia de blastocisto\" class=\"img-left\">\n\n <p>\n Luego, se realiza la FIV y los embriones que alcanzan la etapa de blastocisto (d\u00eda 5-6), mediante un l\u00e1ser especial se realiza un orificio similar al que el embri\u00f3n har\u00e1 en el momento de eclosionar, disminuyendo la posibilidad de da\u00f1o. Posteriormente, se toma una peque\u00f1a muestra de c\u00e9lulas (5-10) del trofectodermo, que formar\u00e1 la placenta, sin afectar su capacidad de desarrollo.\n <\/p>\n\n <p>\n Esa muestra se env\u00eda a un laboratorio especializado que utiliza tecnolog\u00eda de secuenciaci\u00f3n de \u00faltima generaci\u00f3n para evaluar los cromosomas. Solo aquellos embriones con los 46 cromosomas contin\u00faan el an\u00e1lisis para detectar el gen mutado.\n <\/p>\n\n <img data-recalc-dims=\"1\" decoding=\"async\" loading=\"lazy\" src=\"https:\/\/i0.wp.com\/fertility.com.gt\/wp-content\/uploads\/2026\/05\/D758451-scaled.jpg?w=1020&ssl=1\" alt=\"Tecnolog\u00eda gen\u00e9tica avanzada\" class=\"img-right\">\n\n <p><strong>Con este estudio se determina si el embri\u00f3n est\u00e1:<\/strong><\/p>\n <ul>\n <li>Sano<\/li>\n <li>Portador (sin manifestar la enfermedad)<\/li>\n <li>Afectado<\/li>\n <\/ul>\n\n <p>\n Solo se transfieren los embriones libres de la enfermedad y, en algunos casos, seg\u00fan la condici\u00f3n y el consejo gen\u00e9tico, tambi\u00e9n pueden considerarse embriones portadores.\n <\/p>\n\n <p>\n El PGT-M es una herramienta poderosa para prevenir enfermedades hereditarias como fibrosis qu\u00edstica, distrofias musculares, anemia falciforme, enfermedades metab\u00f3licas y epilepsias gen\u00e9ticas, entre muchas otras.\n <\/p>\n\n <p>\n En <strong>Fertility Guatemala<\/strong> acompa\u00f1amos a cada familia desde el estudio inicial hasta la interpretaci\u00f3n detallada de resultados. Combinamos FIV avanzada, gen\u00e9tica de precisi\u00f3n y un apoyo humano cercano para ayudar a lograr un embarazo seguro y un beb\u00e9 sano en casa.\n <\/p>\n\n <div class=\"clear\"><\/div>\n<\/section>\n\n<\/body>\n<\/html>\n\n\n\n<p class=\"wp-block-paragraph\"><\/p>\n","protected":false},"excerpt":{"rendered":"<p>Diagn\u00f3stico gen\u00e9tico preimplantacional para enfermedades monog\u00e9nicas Diagn\u00f3stico gen\u00e9tico preimplantacional para enfermedades monog\u00e9nicas El PGT-M (Preimplantation Genetic Testing for Monogenic Disorders) es una prueba que permite identificar si un embri\u00f3n es portador o est\u00e1 afectado por una enfermedad gen\u00e9tica causada por un solo gen. Su objetivo es ayudar a las familias con riesgo hereditario a tener […]\n","protected":false},"author":1,"featured_media":0,"parent":0,"menu_order":0,"comment_status":"closed","ping_status":"closed","template":"","meta":{"nf_dc_page":"","om_disable_all_campaigns":false,"_monsterinsights_skip_tracking":false,"_monsterinsights_sitenote_active":false,"_monsterinsights_sitenote_note":"","_monsterinsights_sitenote_category":0,"_joinchat":[],"footnotes":""},"class_list":["post-746","page","type-page","status-publish","hentry"],"yoast_head":"\n<title>PGT-M - Fertility Guatemala<\/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:\/\/fertility.com.gt\/es\/pgt-m-2\/\" \/>\n<meta property=\"og:locale\" content=\"es_ES\" \/>\n<meta property=\"og:type\" content=\"article\" \/>\n<meta property=\"og:title\" content=\"PGT-M - Fertility Guatemala\" \/>\n<meta property=\"og:description\" content=\"Diagn\u00f3stico gen\u00e9tico preimplantacional para enfermedades monog\u00e9nicas Diagn\u00f3stico gen\u00e9tico preimplantacional para enfermedades monog\u00e9nicas El PGT-M (Preimplantation Genetic Testing for Monogenic Disorders) es una prueba que permite identificar si un embri\u00f3n es portador o est\u00e1 afectado por una enfermedad gen\u00e9tica causada por un solo gen. 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