{"id":11536,"date":"2025-02-05T22:37:09","date_gmt":"2025-02-05T22:37:09","guid":{"rendered":"https:\/\/emergeamer1dev.wpengine.com\/session\/cracking-the-code-how-genomics-is-transforming-rare-disease-diagnosis-in-children\/"},"modified":"2026-02-20T18:51:20","modified_gmt":"2026-02-20T18:51:20","slug":"cracking-the-code-how-genomics-is-transforming-rare-disease-diagnosis-in-children","status":"publish","type":"session","link":"https:\/\/emergeamericas.com\/es\/session\/cracking-the-code-how-genomics-is-transforming-rare-disease-diagnosis-in-children\/","title":{"rendered":"Descifrando el c\u00f3digo: C\u00f3mo la gen\u00f3mica est\u00e1 transformando el diagn\u00f3stico de las enfermedades raras en los ni\u00f1os"},"content":{"rendered":"","protected":false},"excerpt":{"rendered":"

Para las familias con ni\u00f1os que sufren enfermedades graves e inexplicables, las respuestas pueden parecer inalcanzables, hasta que acuden al Dr. Pankaj Agrawal y a su equipo de UHealth Jackson Children's Care. Mediante la secuenciaci\u00f3n gen\u00e9tica de vanguardia, a menudo con un simple frotis de mejilla, su equipo est\u00e1 resolviendo misterios m\u00e9dicos y diagnosticando dos tercios de las enfermedades raras. Pero su impacto va m\u00e1s all\u00e1 del diagn\u00f3stico: conectan a las familias con la atenci\u00f3n especializada, impulsan la investigaci\u00f3n y ofrecen esperanza donde no la hab\u00eda. \u00danase al Dr. Agrawal y a la Dra. Joanne Ruggiero, Directora General del Holtz Children's Hospital, y comparta con ellos c\u00f3mo est\u00e1n ampliando este innovador programa para llevar la medicina de precisi\u00f3n y las soluciones que cambian vidas a m\u00e1s ni\u00f1os de todo el mundo.<\/p>","protected":false},"featured_media":0,"template":"","meta":{"_acf_changed":false,"_lmt_disableupdate":"","_lmt_disable":"","_links_to":"","_links_to_target":""},"tags":[453],"stage":[468],"topic":[391],"speaker-year":[],"class_list":["post-11536","session","type-session","status-publish","hentry","tag-453","stage-health-hub-stage","topic-healthtech"],"acf":[],"yoast_head":"\nCracking the Code: How Genomics is Transforming Rare Disease Diagnosis in Children - eMerge Americas<\/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:\/\/emergeamericas.com\/es\/session\/cracking-the-code-how-genomics-is-transforming-rare-disease-diagnosis-in-children\/\" \/>\n<meta property=\"og:locale\" content=\"es_ES\" \/>\n<meta property=\"og:type\" content=\"article\" \/>\n<meta property=\"og:title\" content=\"Cracking the Code: How Genomics is Transforming Rare Disease Diagnosis in Children\" \/>\n<meta property=\"og:description\" content=\"For families with children suffering from unexplained and severe conditions, answers can feel out of reach\u2014until they turn to Dr. Pankaj Agrawal and his team at UHealth Jackson Children's Care. Using cutting-edge genetic sequencing, often with just a cheek swab, his team is solving medical mysteries and diagnosing two-thirds of rare conditions. But their impact goes beyond diagnosis\u2014they connect families to specialized care, drive research forward, and offer hope where none existed. 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