{"id":148208,"date":"2025-10-28T15:21:52","date_gmt":"2025-10-28T18:21:52","guid":{"rendered":"http:\/\/ww16.ce.gov.br\/saude\/?p=148208"},"modified":"2025-10-28T16:05:59","modified_gmt":"2025-10-28T19:05:59","slug":"mutirao-genetica-hias-diagnostico-doencas-raras","status":"publish","type":"post","link":"https:\/\/ww16.ce.gov.br\/saude\/2025\/10\/28\/mutirao-genetica-hias-diagnostico-doencas-raras\/","title":{"rendered":"Mutir\u00e3o da Gen\u00e9tica do Hias foca em diagn\u00f3stico precoce e tratamento de doen\u00e7as raras em crian\u00e7as"},"content":{"rendered":"<p style=\"text-align: center\"><img loading=\"lazy\" decoding=\"async\" class=\"aligncenter wp-image-148222 size-full\" src=\"https:\/\/ww16.ce.gov.br\/saude\/wp-content\/uploads\/sites\/64\/2025\/10\/mutirao-genetica-hias-2.png\" alt=\"\" width=\"775\" height=\"485\" srcset=\"https:\/\/ww16.ce.gov.br\/saude\/wp-content\/uploads\/sites\/64\/2025\/10\/mutirao-genetica-hias-2.png 775w, https:\/\/ww16.ce.gov.br\/saude\/wp-content\/uploads\/sites\/64\/2025\/10\/mutirao-genetica-hias-2-600x375.png 600w, https:\/\/ww16.ce.gov.br\/saude\/wp-content\/uploads\/sites\/64\/2025\/10\/mutirao-genetica-hias-2-768x481.png 768w\" sizes=\"auto, (max-width: 775px) 100vw, 775px\" \/><em><span style=\"font-weight: 400\">A\u00e7\u00e3o reuniu 600 fam\u00edlias de todo o Cear\u00e1<\/span><\/em><\/p>\n<p>Para agilizar o <strong>diagn\u00f3stico<\/strong> e o<strong> tratamento<\/strong> de <strong>crian\u00e7as e adolescentes<\/strong> que necessitam de acompanhamento com <strong>geneticista<\/strong>, o <strong>Hospital Infantil Albert Sabin (Hias)<\/strong>, da<strong> Secretaria da Sa\u00fade do Cear\u00e1 (Sesa)<\/strong>, realizou no \u00faltimo s\u00e1bado (25) mais uma edi\u00e7\u00e3o do <strong>Mutir\u00e3o da Gen\u00e9tica<\/strong>.<\/p>\n<p>A a\u00e7\u00e3o reuniu cerca de 600 fam\u00edlias de diversas regi\u00f5es do estado, com destaque para as macrorregi\u00f5es Cariri e Norte. Os pacientes foram previamente contactados pela Central de Regula\u00e7\u00e3o do Estado, com o intuito de garantir a organiza\u00e7\u00e3o do atendimento.<\/p>\n<p><img loading=\"lazy\" decoding=\"async\" class=\"size-medium wp-image-148211 alignleft\" style=\"font-family: OpenSans-Light, Helvetica, Arial, sans-serif;font-size: 14px;letter-spacing: 0.02px\" src=\"https:\/\/ww16.ce.gov.br\/saude\/wp-content\/uploads\/sites\/64\/2025\/10\/mutirao-genetica-hias-1-600x375.png\" alt=\"\" width=\"368\" height=\"230\" srcset=\"https:\/\/ww16.ce.gov.br\/saude\/wp-content\/uploads\/sites\/64\/2025\/10\/mutirao-genetica-hias-1-600x375.png 600w, https:\/\/ww16.ce.gov.br\/saude\/wp-content\/uploads\/sites\/64\/2025\/10\/mutirao-genetica-hias-1-768x481.png 768w, https:\/\/ww16.ce.gov.br\/saude\/wp-content\/uploads\/sites\/64\/2025\/10\/mutirao-genetica-hias-1.png 775w\" sizes=\"auto, (max-width: 368px) 100vw, 368px\" \/><\/p>\n<p>Entre as fam\u00edlias atendidas est\u00e1 a de Alexandre (foto), 10 anos, morador de Guaraciaba do Norte. Ele viajou com a m\u00e3e, Cleane C\u00e9sar, 42, dona de casa, em busca da consulta t\u00e3o aguardada. \u201cEle tem macrocefalia, escoliose, hipotonia (diminui\u00e7\u00e3o do t\u00f4nus, moleza) e autismo\u201d, detalha.<\/p>\n<p>\u201cEst\u00e1vamos sendo acompanhados pela Rede Sarah, no Rio de Janeiro, e quando voltamos para o Cear\u00e1 entramos na fila do Hias. Agora, com o mutir\u00e3o, passamos pela triagem e j\u00e1 vamos marcar a consulta. Estou feliz, mas ansiosa. Torcendo para que tudo esteja bem com ele\u201d, contou.<\/p>\n<p>O mutir\u00e3o teve como foco <strong>reduzir o tempo de espera por consultas<\/strong> e <strong>fortalecer o diagn\u00f3stico precoce de doen\u00e7as gen\u00e9ticas<\/strong>. As avalia\u00e7\u00f5es foram conduzidas por uma equipe multiprofissional formada por geneticistas, pediatras, enfermeiros e profissionais administrativos.<\/p>\n<p style=\"text-align: center\"><img loading=\"lazy\" decoding=\"async\" class=\"aligncenter wp-image-148210 size-full\" src=\"https:\/\/ww16.ce.gov.br\/saude\/wp-content\/uploads\/sites\/64\/2025\/10\/mutirao-genetica-hias.png\" alt=\"\" width=\"775\" height=\"485\" srcset=\"https:\/\/ww16.ce.gov.br\/saude\/wp-content\/uploads\/sites\/64\/2025\/10\/mutirao-genetica-hias.png 775w, https:\/\/ww16.ce.gov.br\/saude\/wp-content\/uploads\/sites\/64\/2025\/10\/mutirao-genetica-hias-600x375.png 600w, https:\/\/ww16.ce.gov.br\/saude\/wp-content\/uploads\/sites\/64\/2025\/10\/mutirao-genetica-hias-768x481.png 768w\" sizes=\"auto, (max-width: 775px) 100vw, 775px\" \/> <em>Profissionais do Hias realizaram triagens e consultas especializadas para acelerar diagn\u00f3sticos e encaminhamentos<\/em><\/p>\n<p>A geneticista Erlane Ribeiro, do Hias, destaca a relev\u00e2ncia do diagn\u00f3stico precoce. \u201cAinda h\u00e1 desconhecimento entre profissionais da sa\u00fade sobre quando encaminhar pacientes \u00e0 gen\u00e9tica, e esse tipo de a\u00e7\u00e3o ajuda a ampliar essa rede de cuidado. Muitas doen\u00e7as gen\u00e9ticas, se n\u00e3o forem identificadas a tempo, acabam tendo tratamentos menos eficazes. <strong>O diagn\u00f3stico precoce \u00e9 sempre o melhor caminho<\/strong>\u201d, afirma.<\/p>\n<p>Durante o mutir\u00e3o, os profissionais avaliaram casos de diferentes n\u00edveis de complexidade e definiram encaminhamentos para acompanhamento cont\u00ednuo. De Tiangu\u00e1, a dona de casa Maria Soares, 32, levou o filho Eliazaf, de 5 anos, para a triagem. A fam\u00edlia tem hist\u00f3rico de S\u00edndrome de Marfan, condi\u00e7\u00e3o gen\u00e9tica rara que afeta o tecido conjuntivo, respons\u00e1vel por dar sustenta\u00e7\u00e3o e elasticidade aos \u00f3rg\u00e3os e sistemas do corpo.<\/p>\n<p>\u201cA agente de sa\u00fade chegou na minha porta e avisou que passar\u00edamos por essa triagem. Meus filhos eram atendidos por pediatras no munic\u00edpio, mas agora poder\u00e3o ser acompanhados por um especialista\u201d, relata.<\/p>\n","protected":false},"excerpt":{"rendered":"<p>A\u00e7\u00e3o reuniu 600 fam\u00edlias de todo o Cear\u00e1 Para agilizar o diagn\u00f3stico e o tratamento de crian\u00e7as e adolescentes que necessitam de acompanhamento com geneticista, o Hospital Infantil Albert Sabin (Hias), da Secretaria da Sa\u00fade do Cear\u00e1 (Sesa), realizou no \u00faltimo s\u00e1bado (25) mais uma edi\u00e7\u00e3o do Mutir\u00e3o da Gen\u00e9tica. A a\u00e7\u00e3o reuniu cerca de [&hellip;]<\/p>\n","protected":false},"author":767,"featured_media":148222,"comment_status":"closed","ping_status":"closed","sticky":false,"template":"","format":"standard","meta":{"_acf_changed":false,"inline_featured_image":false,"footnotes":""},"categories":[498],"tags":[3917,2211,689,3267,753,4505],"class_list":["post-148208","post","type-post","status-publish","format-standard","has-post-thumbnail","hentry","category-hias","tag-diagnostico-precoce","tag-doencas-raras","tag-hias","tag-hospital-infantil-albert-sabin-hias","tag-mutirao","tag-mutirao-de-genetica"],"acf":[],"yoast_head":"<!-- This site is optimized with the Yoast SEO plugin v26.9 - https:\/\/yoast.com\/product\/yoast-seo-wordpress\/ -->\n<title>Mutir\u00e3o da Gen\u00e9tica foca em diagn\u00f3stico e tratamento de doen\u00e7as raras em crian\u00e7as<\/title>\n<meta name=\"description\" content=\"O Hospital Infantil Albert Sabin (Hias) realizou, no \u00faltimo s\u00e1bado (25), mais uma edi\u00e7\u00e3o do Mutir\u00e3o da Gen\u00e9tica para agilizar o diagn\u00f3stico e o tratamento de crian\u00e7as e adolescentes com suspeita de doen\u00e7as raras em todo o Cear\u00e1. 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