{"id":5529,"date":"2024-05-15T14:31:00","date_gmt":"2024-05-15T20:31:00","guid":{"rendered":"https:\/\/diarioabcdemichoacan.com.mx\/lasnoticias\/?p=5529"},"modified":"2024-05-15T14:32:29","modified_gmt":"2024-05-15T20:32:29","slug":"conmemoran-dia-mundial-de-la-mucopolisacaridosis","status":"publish","type":"post","link":"https:\/\/diarioabcdemichoacan.com.mx\/lasnoticias\/conmemoran-dia-mundial-de-la-mucopolisacaridosis\/","title":{"rendered":"Conmemoran D\u00eda Mundial de la Mucopolisacaridosis."},"content":{"rendered":"<h2>Enfermedad rara lisosomal diagnosticada en 300 personas en M\u00e9xico de los cuales de 12 a 15 est\u00e1n en Michoac\u00e1n.<\/h2>\n<ul>\n<li>Visibilizarla y brindar la informaci\u00f3n correcta sobre la enfermedad, el objetivo.<\/li>\n<\/ul>\n<p>&nbsp;<\/p>\n<h6>POR REDACCI\u00d3N, DIARIO ABC DE MICHOAC\u00c1N, 15 DE MAYO DE 2024.<\/h6>\n<hr \/>\n<p>Morelia, Mich. &#8211; En el marco del D\u00eda Mundial de la Mucopolisacaridosis (MPS), que se celebra cada 15 de mayo, el Ayuntamiento de Morelia, a trav\u00e9s de la Comisi\u00f3n de la Mujer, Derechos Humanos y Grupos de Situaci\u00f3n de Vulnerabilidad, en encabeza la regidora, Paulina Mungu\u00eda Su\u00e1rez y la Asociaci\u00f3n Mexicana de Enfermedades Raras (AMAER), se unieron a la conmemoraci\u00f3n de esta enfermedad rara que afecta a un n\u00famero significativo de personas en nuestro pa\u00eds.<\/p>\n<p>&nbsp;<\/p>\n<p>Destacar que la MPS es una enfermedad lisosomal rara, caracterizada por la deficiencia de enzimas, que se manifiesta en la infancia y progresa con el tiempo, generando complicaciones que pueden afectar gravemente la calidad de vida y la esperanza de vida de quienes la padecen.<\/p>\n<p>&nbsp;<\/p>\n<p><img loading=\"lazy\" decoding=\"async\" class=\"alignnone size-medium wp-image-5532\" src=\"https:\/\/diarioabcdemichoacan.com.mx\/lasnoticias\/wp-content\/uploads\/2024\/05\/WhatsApp-Image-2024-05-15-at-2.24.03-PM-1-500x333.jpeg\" alt=\"\" width=\"500\" height=\"333\" srcset=\"https:\/\/diarioabcdemichoacan.com.mx\/lasnoticias\/wp-content\/uploads\/2024\/05\/WhatsApp-Image-2024-05-15-at-2.24.03-PM-1-500x333.jpeg 500w, https:\/\/diarioabcdemichoacan.com.mx\/lasnoticias\/wp-content\/uploads\/2024\/05\/WhatsApp-Image-2024-05-15-at-2.24.03-PM-1-1024x682.jpeg 1024w, https:\/\/diarioabcdemichoacan.com.mx\/lasnoticias\/wp-content\/uploads\/2024\/05\/WhatsApp-Image-2024-05-15-at-2.24.03-PM-1-768x512.jpeg 768w, https:\/\/diarioabcdemichoacan.com.mx\/lasnoticias\/wp-content\/uploads\/2024\/05\/WhatsApp-Image-2024-05-15-at-2.24.03-PM-1-1536x1023.jpeg 1536w, https:\/\/diarioabcdemichoacan.com.mx\/lasnoticias\/wp-content\/uploads\/2024\/05\/WhatsApp-Image-2024-05-15-at-2.24.03-PM-1-150x100.jpeg 150w, https:\/\/diarioabcdemichoacan.com.mx\/lasnoticias\/wp-content\/uploads\/2024\/05\/WhatsApp-Image-2024-05-15-at-2.24.03-PM-1-300x200.jpeg 300w, https:\/\/diarioabcdemichoacan.com.mx\/lasnoticias\/wp-content\/uploads\/2024\/05\/WhatsApp-Image-2024-05-15-at-2.24.03-PM-1-696x464.jpeg 696w, https:\/\/diarioabcdemichoacan.com.mx\/lasnoticias\/wp-content\/uploads\/2024\/05\/WhatsApp-Image-2024-05-15-at-2.24.03-PM-1-1068x712.jpeg 1068w, https:\/\/diarioabcdemichoacan.com.mx\/lasnoticias\/wp-content\/uploads\/2024\/05\/WhatsApp-Image-2024-05-15-at-2.24.03-PM-1.jpeg 1600w\" sizes=\"auto, (max-width: 500px) 100vw, 500px\" \/><\/p>\n<p>&nbsp;<\/p>\n<p>Al respecto y seg\u00fan datos recientes proporcionados durante una rueda de prensa realizada este mi\u00e9rcoles en palacio municipal, el Dr. Luis Figuera, m\u00e9dico genetista en el Centro de Investigaci\u00f3n Biom\u00e9dica del IMSS en Guadalajara, inform\u00f3 que se estima que alrededor de 300 personas en M\u00e9xico padecen de esta condici\u00f3n, de las cuales entre 12 a 15 residen en Michoac\u00e1n.<\/p>\n<p>&nbsp;<\/p>\n<p>Asimismo, explic\u00f3 que las enfermedades raras como la MPS presentan desaf\u00edos \u00fanicos, tanto en el diagn\u00f3stico como en el tratamiento, y destac\u00f3 la importancia del apoyo m\u00e9dico y la sensibilizaci\u00f3n p\u00fablica.<\/p>\n<p>&nbsp;<\/p>\n<p><img loading=\"lazy\" decoding=\"async\" class=\"alignnone size-medium wp-image-5531\" src=\"https:\/\/diarioabcdemichoacan.com.mx\/lasnoticias\/wp-content\/uploads\/2024\/05\/WhatsApp-Image-2024-05-15-at-2.24.03-PM-2-500x353.jpeg\" alt=\"\" width=\"500\" height=\"353\" srcset=\"https:\/\/diarioabcdemichoacan.com.mx\/lasnoticias\/wp-content\/uploads\/2024\/05\/WhatsApp-Image-2024-05-15-at-2.24.03-PM-2-500x353.jpeg 500w, https:\/\/diarioabcdemichoacan.com.mx\/lasnoticias\/wp-content\/uploads\/2024\/05\/WhatsApp-Image-2024-05-15-at-2.24.03-PM-2-768x542.jpeg 768w, https:\/\/diarioabcdemichoacan.com.mx\/lasnoticias\/wp-content\/uploads\/2024\/05\/WhatsApp-Image-2024-05-15-at-2.24.03-PM-2-150x106.jpeg 150w, https:\/\/diarioabcdemichoacan.com.mx\/lasnoticias\/wp-content\/uploads\/2024\/05\/WhatsApp-Image-2024-05-15-at-2.24.03-PM-2-300x212.jpeg 300w, https:\/\/diarioabcdemichoacan.com.mx\/lasnoticias\/wp-content\/uploads\/2024\/05\/WhatsApp-Image-2024-05-15-at-2.24.03-PM-2-696x491.jpeg 696w, https:\/\/diarioabcdemichoacan.com.mx\/lasnoticias\/wp-content\/uploads\/2024\/05\/WhatsApp-Image-2024-05-15-at-2.24.03-PM-2.jpeg 981w\" sizes=\"auto, (max-width: 500px) 100vw, 500px\" \/><\/p>\n<p>&nbsp;<\/p>\n<p>Ante dichos datos, la regidora Paulina Mungu\u00eda enfatiz\u00f3 la necesidad de brindar informaci\u00f3n precisa y actualizada sobre la MPS, con el objetivo de erradicar la desinformaci\u00f3n y promover una mayor conciencia sobre esta enfermedad. \u201cQueremos tener la responsabilidad de que hoy se hable realmente de qu\u00e9 es la mucopolisacaridosis como una variante de una enfermedad rara\u201d, se\u00f1al\u00f3.<\/p>\n<p>&nbsp;<\/p>\n<p>Por su parte, Leonardo Rojas, miembro fundador de la Asociaci\u00f3n Mexicana de Enfermedades Raras (AMAER), destac\u00f3 el papel crucial de las organizaciones de apoyo en la b\u00fasqueda de soluciones y la creaci\u00f3n de conciencia sobre las enfermedades raras, incluida la MPS.<\/p>\n<p>&nbsp;<\/p>\n<p><img loading=\"lazy\" decoding=\"async\" class=\"alignnone size-medium wp-image-5533\" src=\"https:\/\/diarioabcdemichoacan.com.mx\/lasnoticias\/wp-content\/uploads\/2024\/05\/WhatsApp-Image-2024-05-15-at-2.24.03-PM-500x383.jpeg\" alt=\"\" width=\"500\" height=\"383\" srcset=\"https:\/\/diarioabcdemichoacan.com.mx\/lasnoticias\/wp-content\/uploads\/2024\/05\/WhatsApp-Image-2024-05-15-at-2.24.03-PM-500x383.jpeg 500w, https:\/\/diarioabcdemichoacan.com.mx\/lasnoticias\/wp-content\/uploads\/2024\/05\/WhatsApp-Image-2024-05-15-at-2.24.03-PM-1024x785.jpeg 1024w, https:\/\/diarioabcdemichoacan.com.mx\/lasnoticias\/wp-content\/uploads\/2024\/05\/WhatsApp-Image-2024-05-15-at-2.24.03-PM-768x589.jpeg 768w, https:\/\/diarioabcdemichoacan.com.mx\/lasnoticias\/wp-content\/uploads\/2024\/05\/WhatsApp-Image-2024-05-15-at-2.24.03-PM-150x115.jpeg 150w, https:\/\/diarioabcdemichoacan.com.mx\/lasnoticias\/wp-content\/uploads\/2024\/05\/WhatsApp-Image-2024-05-15-at-2.24.03-PM-300x230.jpeg 300w, https:\/\/diarioabcdemichoacan.com.mx\/lasnoticias\/wp-content\/uploads\/2024\/05\/WhatsApp-Image-2024-05-15-at-2.24.03-PM-696x534.jpeg 696w, https:\/\/diarioabcdemichoacan.com.mx\/lasnoticias\/wp-content\/uploads\/2024\/05\/WhatsApp-Image-2024-05-15-at-2.24.03-PM-1068x819.jpeg 1068w, https:\/\/diarioabcdemichoacan.com.mx\/lasnoticias\/wp-content\/uploads\/2024\/05\/WhatsApp-Image-2024-05-15-at-2.24.03-PM.jpeg 1390w\" sizes=\"auto, (max-width: 500px) 100vw, 500px\" \/><\/p>\n<p>&nbsp;<\/p>\n<p>Esa as\u00ed que, durante la rueda de prensa, Osmara Sayuri Maciel Color, madre de Iker Leonardo V., ni\u00f1o con MPS, comparti\u00f3 su experiencia personal, subrayando las dificultades que enfrentan las familias afectadas debido a la falta de comprensi\u00f3n y apoyo en la sociedad, y subray\u00f3 que por ello, es fundamental que se visibilice m\u00e1s esta enfermedad.<\/p>\n<p>&nbsp;<\/p>\n<p>Destacar que en el marco de esta conmemoraci\u00f3n, se enfatiza la importancia del tamizaje temprano para detectar la MPS en etapas iniciales, lo que puede mejorar significativamente las perspectivas de tratamiento y calidad de vida de los pacientes.<\/p>\n<p>&nbsp;<\/p>\n<p>En apego a las acciones preventivas implementadas por la Administraci\u00f3n Municipal, en raz\u00f3n de las disposiciones emitidas por las autoridades electorales, este contenido tiene fines informativos.<\/p>\n","protected":false},"excerpt":{"rendered":"<p>Enfermedad rara lisosomal diagnosticada en 300 personas en M\u00e9xico de los cuales de 12 a 15 est\u00e1n en Michoac\u00e1n. Visibilizarla y brindar la informaci\u00f3n correcta sobre la enfermedad, el objetivo. &nbsp; POR REDACCI\u00d3N, DIARIO ABC DE MICHOAC\u00c1N, 15 DE MAYO DE 2024. Morelia, Mich. &#8211; En el marco del D\u00eda Mundial de la Mucopolisacaridosis (MPS), [&hellip;]<\/p>\n","protected":false},"author":9,"featured_media":5530,"comment_status":"closed","ping_status":"closed","sticky":false,"template":"","format":"standard","meta":{"footnotes":""},"categories":[18,7,27],"tags":[],"class_list":{"0":"post-5529","1":"post","2":"type-post","3":"status-publish","4":"format-standard","5":"has-post-thumbnail","7":"category-ayuntamiento-de-morelia","8":"category-morelia","9":"category-slider"},"yoast_head":"<!-- This site is optimized with the Yoast SEO plugin v24.0 - https:\/\/yoast.com\/wordpress\/plugins\/seo\/ -->\n<title>Conmemoran D\u00eda Mundial de la Mucopolisacaridosis. - Diario ABC de Michoac\u00e1n<\/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:\/\/diarioabcdemichoacan.com.mx\/lasnoticias\/conmemoran-dia-mundial-de-la-mucopolisacaridosis\/\" \/>\n<meta property=\"og:locale\" content=\"es_ES\" \/>\n<meta property=\"og:type\" content=\"article\" \/>\n<meta property=\"og:title\" content=\"Conmemoran D\u00eda Mundial de la Mucopolisacaridosis. - Diario ABC de Michoac\u00e1n\" \/>\n<meta property=\"og:description\" content=\"Enfermedad rara lisosomal diagnosticada en 300 personas en M\u00e9xico de los cuales de 12 a 15 est\u00e1n en Michoac\u00e1n. Visibilizarla y brindar la informaci\u00f3n correcta sobre la enfermedad, el objetivo. &nbsp; POR REDACCI\u00d3N, DIARIO ABC DE MICHOAC\u00c1N, 15 DE MAYO DE 2024. 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