{"id":755,"date":"2013-03-11T11:41:44","date_gmt":"2013-03-11T15:41:44","guid":{"rendered":"http:\/\/medicina.udd.cl\/centro-genetica-humana\/?p=755"},"modified":"2013-03-15T08:15:02","modified_gmt":"2013-03-15T12:15:02","slug":"sindrome-velocardiofacial-prioridad-tratar-a-tiempo-problemas-del-habla","status":"publish","type":"post","link":"https:\/\/medicina.udd.cl\/centro-genetica-genomica\/noticias\/2013\/03\/11\/sindrome-velocardiofacial-prioridad-tratar-a-tiempo-problemas-del-habla\/","title":{"rendered":"S\u00edndrome Velocardiofacial: prioridad tratar a tiempo problemas del habla"},"content":{"rendered":"<div id=\"gallery-1\" class=\"carousel slide carousel-gallery\" data-ride=\"false\" data-interval=\"false\"><div class=\"carousel-inner\" role=\"listbox\"><figure class=\"carousel-item active\"><img loading=\"lazy\" decoding=\"async\" width=\"640\" height=\"440\" src=\"https:\/\/medicina.udd.cl\/centro-genetica-genomica\/files\/2013\/03\/Dr.-Antonio-Ysunza.jpg\" class=\"attachment-landscape_952 size-landscape_952\" alt=\"\" srcset=\"https:\/\/medicina.udd.cl\/centro-genetica-genomica\/files\/2013\/03\/Dr.-Antonio-Ysunza.jpg 640w, https:\/\/medicina.udd.cl\/centro-genetica-genomica\/files\/2013\/03\/Dr.-Antonio-Ysunza-300x206.jpg 300w\" sizes=\"auto, (max-width: 640px) 100vw, 640px\" \/><\/figure><figure class=\"carousel-item\"><img loading=\"lazy\" decoding=\"async\" width=\"640\" height=\"426\" src=\"https:\/\/medicina.udd.cl\/centro-genetica-genomica\/files\/2013\/03\/Dra.-Marcela-Llorente.jpg\" class=\"attachment-landscape_952 size-landscape_952\" alt=\"\" srcset=\"https:\/\/medicina.udd.cl\/centro-genetica-genomica\/files\/2013\/03\/Dra.-Marcela-Llorente.jpg 640w, https:\/\/medicina.udd.cl\/centro-genetica-genomica\/files\/2013\/03\/Dra.-Marcela-Llorente-300x200.jpg 300w\" sizes=\"auto, (max-width: 640px) 100vw, 640px\" \/><\/figure><figure class=\"carousel-item\"><img loading=\"lazy\" decoding=\"async\" width=\"640\" height=\"427\" src=\"https:\/\/medicina.udd.cl\/centro-genetica-genomica\/files\/2013\/03\/Asistentes-jornada-S\u00edndrome-VCF.jpg\" class=\"attachment-landscape_952 size-landscape_952\" alt=\"\" srcset=\"https:\/\/medicina.udd.cl\/centro-genetica-genomica\/files\/2013\/03\/Asistentes-jornada-S\u00edndrome-VCF.jpg 640w, https:\/\/medicina.udd.cl\/centro-genetica-genomica\/files\/2013\/03\/Asistentes-jornada-S\u00edndrome-VCF-300x200.jpg 300w\" sizes=\"auto, (max-width: 640px) 100vw, 640px\" \/><\/figure><figure class=\"carousel-item\"><img loading=\"lazy\" decoding=\"async\" width=\"640\" height=\"427\" src=\"https:\/\/medicina.udd.cl\/centro-genetica-genomica\/files\/2013\/03\/Equipo-Centro-Gen\u00e9tica-en-recepci\u00f3n.jpg\" class=\"attachment-landscape_952 size-landscape_952\" alt=\"\" srcset=\"https:\/\/medicina.udd.cl\/centro-genetica-genomica\/files\/2013\/03\/Equipo-Centro-Gen\u00e9tica-en-recepci\u00f3n.jpg 640w, https:\/\/medicina.udd.cl\/centro-genetica-genomica\/files\/2013\/03\/Equipo-Centro-Gen\u00e9tica-en-recepci\u00f3n-300x200.jpg 300w\" sizes=\"auto, (max-width: 640px) 100vw, 640px\" \/><\/figure><figure class=\"carousel-item\"><img loading=\"lazy\" decoding=\"async\" width=\"640\" height=\"427\" src=\"https:\/\/medicina.udd.cl\/centro-genetica-genomica\/files\/2013\/03\/Paciente-S\u00edndrome-VCF-pintando.jpg\" class=\"attachment-landscape_952 size-landscape_952\" alt=\"\" srcset=\"https:\/\/medicina.udd.cl\/centro-genetica-genomica\/files\/2013\/03\/Paciente-S\u00edndrome-VCF-pintando.jpg 640w, https:\/\/medicina.udd.cl\/centro-genetica-genomica\/files\/2013\/03\/Paciente-S\u00edndrome-VCF-pintando-300x200.jpg 300w\" sizes=\"auto, (max-width: 640px) 100vw, 640px\" \/><\/figure><figure class=\"carousel-item\"><img loading=\"lazy\" decoding=\"async\" width=\"640\" height=\"405\" src=\"https:\/\/medicina.udd.cl\/centro-genetica-genomica\/files\/2013\/03\/Voluntarias-y-ni\u00f1os-S\u00edndrome-VCF.jpg\" class=\"attachment-landscape_952 size-landscape_952\" alt=\"\" srcset=\"https:\/\/medicina.udd.cl\/centro-genetica-genomica\/files\/2013\/03\/Voluntarias-y-ni\u00f1os-S\u00edndrome-VCF.jpg 640w, https:\/\/medicina.udd.cl\/centro-genetica-genomica\/files\/2013\/03\/Voluntarias-y-ni\u00f1os-S\u00edndrome-VCF-300x190.jpg 300w, https:\/\/medicina.udd.cl\/centro-genetica-genomica\/files\/2013\/03\/Voluntarias-y-ni\u00f1os-S\u00edndrome-VCF-125x80.jpg 125w\" sizes=\"auto, (max-width: 640px) 100vw, 640px\" \/><\/figure><figure class=\"carousel-item\"><img loading=\"lazy\" decoding=\"async\" width=\"640\" height=\"455\" src=\"https:\/\/medicina.udd.cl\/centro-genetica-genomica\/files\/2013\/03\/Voluntarias-y-ni\u00f1a-VCF.jpg\" class=\"attachment-landscape_952 size-landscape_952\" alt=\"\" srcset=\"https:\/\/medicina.udd.cl\/centro-genetica-genomica\/files\/2013\/03\/Voluntarias-y-ni\u00f1a-VCF.jpg 640w, https:\/\/medicina.udd.cl\/centro-genetica-genomica\/files\/2013\/03\/Voluntarias-y-ni\u00f1a-VCF-300x213.jpg 300w, https:\/\/medicina.udd.cl\/centro-genetica-genomica\/files\/2013\/03\/Voluntarias-y-ni\u00f1a-VCF-316x224.jpg 316w, https:\/\/medicina.udd.cl\/centro-genetica-genomica\/files\/2013\/03\/Voluntarias-y-ni\u00f1a-VCF-87x62.jpg 87w\" sizes=\"auto, (max-width: 640px) 100vw, 640px\" \/><\/figure><figure class=\"carousel-item\"><img loading=\"lazy\" decoding=\"async\" width=\"640\" height=\"423\" src=\"https:\/\/medicina.udd.cl\/centro-genetica-genomica\/files\/2013\/03\/Voluntario-y-ni\u00f1os-VCF.jpg\" class=\"attachment-landscape_952 size-landscape_952\" alt=\"\" srcset=\"https:\/\/medicina.udd.cl\/centro-genetica-genomica\/files\/2013\/03\/Voluntario-y-ni\u00f1os-VCF.jpg 640w, https:\/\/medicina.udd.cl\/centro-genetica-genomica\/files\/2013\/03\/Voluntario-y-ni\u00f1os-VCF-300x198.jpg 300w\" sizes=\"auto, (max-width: 640px) 100vw, 640px\" \/><\/figure><\/div><footer class=\"carousel-footer\"><div class=\"carousel-counter\"><span class=\"carousel-counter-current\"><\/span> \/ <span class=\"carousel-counter-total\"><\/span><\/div><a class=\"carousel-control-prev\" href=\"#gallery-1\" role=\"button\" data-slide=\"prev\"><svg aria-hidden=\"true\" class=\"svg-chevron-left-dims\"><use xlink:href='https:\/\/medicina.udd.cl\/centro-genetica-genomica\/wp-content\/themes\/facultades-2018\/assets\/img\/svg\/dist\/main.svg?version=1695853099#chevron-left'><\/use><\/svg><span class=\"sr-only\">Anterior<\/span><\/a><a class=\"carousel-control-next\" href=\"#gallery-1\" role=\"button\" data-slide=\"next\"><svg aria-hidden=\"true\" class=\"svg-chevron-right-dims\"><use xlink:href='https:\/\/medicina.udd.cl\/centro-genetica-genomica\/wp-content\/themes\/facultades-2018\/assets\/img\/svg\/dist\/main.svg?version=1695853099#chevron-right'><\/use><\/svg><span class=\"sr-only\">Siguiente<\/span><\/a><\/footer><\/div>\n<p>El <strong>doctor Antonio Ysunza, del Hospital Beaumont de Michigan (EEUU)<\/strong>, explic\u00f3 que as\u00ed como el tratamiento de las afecciones cardiacas es fundamental para el buen desarrollo de los pacientes con <strong>S\u00edndrome Velocardiofacial (VCF)<\/strong>, tambi\u00e9n lo es la terapia fonoaudiol\u00f3gica, ya que gran parte de los ni\u00f1os nace con una fisura de paladar que afecta el habla.<\/p>\n<p>El m\u00e9dico fue el orador central de la<strong> IV Jornada de Actualizaci\u00f3n en Tratamiento del S\u00edndrome VCF<\/strong>, que se desarroll\u00f3 el s\u00e1bado \u00faltimo en el Aula Magna de la Facultad de Medicina CAS-UDD, organizada por el Centro de Gen\u00e9tica Humana.<\/p>\n<p>Ysunza enfatiz\u00f3 que no es suficiente que se revise el paladar del ni\u00f1o en forma visual. Hace falta tocarlo \u201cporque muchos de los pacientes con el s\u00edndrome tienen una fisura submucosa y entonces no se ve\u201d y luego \u201cescuchar al ni\u00f1o, haciendo que emita sonidos que hagan presi\u00f3n sobre el paladar, como es el caso de la p, k y la s\u201d, agreg\u00f3.<\/p>\n<p>Sin el tratamiento adecuado y oportuno, los ni\u00f1os tendr\u00e1n dificultades para comunicarse, eso impactar\u00e1 en su desempe\u00f1o escolar, sufrir\u00e1n frustraci\u00f3n e incluso pueden ser objeto de burlas de los otros menores, advirti\u00f3 el doctor.<\/p>\n<p>Uno de cada 4.000 reci\u00e9n nacidos en el pa\u00eds sufre S\u00edndrome VCF o S\u00edndrome de Microdeleci\u00f3n 22q11. Es la segunda enfermedad de origen cromos\u00f3mico de mayor incidencia en el pa\u00eds, despu\u00e9s del S\u00edndrome de Down.<\/p>\n<p>En el encuentro participaron tambi\u00e9n la doctora <strong>Marcela Llorente<\/strong>, Inmun\u00f3loga Infantil y docente de la Facultad, y la doctora <strong>Gabriela Repetto <\/strong>\u2013pediatra y genetista, directora del Centro de Gen\u00e9tica Humana-, adem\u00e1s de la psiquiatra <strong>Rosemarie Fritsch.<\/strong><\/p>\n<p>Mientras sus padres asist\u00edan a la jornada, los ni\u00f1os jugaron y fueron cuidados por voluntarios-monitores de las distintas carreras de la Facultad.<\/p>\n","protected":false},"excerpt":{"rendered":"<p>Expertos en esta enfermedad se reunieron en la Facultad de Medicina CAS-UDD.<\/p>\n","protected":false},"author":1,"featured_media":0,"comment_status":"open","ping_status":"open","sticky":false,"template":"","format":"standard","meta":{"footnotes":""},"categories":[4],"tags":[],"class_list":["post-755","post","type-post","status-publish","format-standard","hentry","category-noticias"],"yoast_head":"<!-- This site is optimized with the Yoast SEO plugin v26.9 - 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