{"id":26,"date":"2026-05-26T13:39:51","date_gmt":"2026-05-26T13:39:51","guid":{"rendered":"https:\/\/www.ultraconecta.com\/ar\/?page_id=26"},"modified":"2026-10-05T15:39:00","modified_gmt":"2026-10-05T15:39:00","slug":"home","status":"publish","type":"page","link":"https:\/\/www.ultraconecta.com\/ar\/","title":{"rendered":"Home"},"content":{"rendered":"<p><!-- HERO SECTION --><\/p>\n<section class=\"hero\">\n<div class=\"container\">\n<div class=\"hero__grid\">\n      <!-- Left card: Intro + image --><\/p>\n<article class=\"hero-card hero-card--intro\">\n<figure class=\"hero-card__media\">\n          <img decoding=\"async\" fetchpriority=\"high\"\n            src=\"\/ar\/wp-content\/uploads\/Bastian-conviviendo-con.webp\"\n            alt=\"Bastian, paciente XLH sentado en el regazo de su mam\u00e1, ambos est\u00e1n sonriendo\"   width=\"444\" height=\"677\"\n          \/><figcaption class=\"hero-card__caption\">\n               Bastian y su mam\u00e1<br \/>\n          <\/figcaption><\/figure>\n<div class=\"hero-card__body\">\n<h1 class=\"hero-card__title\">\n            Hipofosfatemia ligada al cromosoma X (XLH)<br \/>\n          <\/h1>\n<p class=\"hero-card__text\">\n            XLH es una<br \/>\n            <strong>enfermedad hereditaria, progresiva y cr\u00f3nica<\/strong> que<br \/>\n            afecta tanto a ni\u00f1os como a adultos.<br \/> Obten\u00e9 m\u00e1s informaci\u00f3n sobre XLH,<br \/>\n              sus signos y s\u00edntomas y el manejo de esta enfermedad poco frecuente.\n          <\/p>\n<div class=\"hero-card__actions\">\n            <a\n              class=\"btn btn--pill btn--purple\"\n              href=\"https:\/\/www.ultraconecta.com\/ar\/acerca-de-xlh\/\"\n              >m\u00e1s informaci\u00f3n sobre XLH<\/a\n            ><br \/>\n            <a\n              class=\"btn btn--pill btn--outline\"\n              href=\"https:\/\/www.ultraconecta.com\/ar\/signos-y-sintomas-ninos\/\"\n              >Ver signos y s\u00edntomas<\/a\n            >\n          <\/div>\n<\/p><\/div>\n<\/article>\n<p>      <!-- Right card: Patient story --><\/p>\n<article class=\"hero-card hero-card--story\">\n<div class=\"hero-card__video\">\n          <img decoding=\"async\"\nfetchpriority=\"high\"\nwidth=\"732\"\nheight=\"458\"\n            src=\"\/ar\/wp-content\/uploads\/Background-1.webp\"\n            alt=\"Silvia, paciente XLH, sonriendo\"\n          \/><br \/>\n          &nbsp;\n        <\/div>\n<div class=\"hero-card__name-bar\">\n<div class=\"site-header__accentNew\" aria-hidden=\"true\">\n            <span class=\"site-header__accent-blue\"><\/span><br \/>\n            <span class=\"site-header__accent-yellow\"><\/span>\n          <\/div>\n<p>          <span class=\"hero-card__name-accent\" aria-hidden=\"true\"> <\/span><\/p>\n<div class=\"hero-card__name-text\">\n<h2 class=\"hero-card__name\">Silvia<\/h2>\n<\/p><\/div>\n<\/p><\/div>\n<div class=\"hero-card__story-body\">\n<blockquote class=\"hero-card__quote\"><p>\n\u201cYo ten\u00eda 5 a\u00f1os cuando me diagnosticaron una enfermedad rara: raquitismo hipofosfat\u00e9mico,\u00a0una enfermedad que casi no se pod\u00eda pronunciar.\u201d\n          <\/p><\/blockquote>\n<p class=\"hero-card__text\">\n            XLH puede ser una enfermedad poco<br \/>\n             frecuente, pero no est\u00e1s solo. Descubr\u00ed<br \/>\n             c\u00f3mo conviven otras personas con XLH.\n          <\/p>\n<div class=\"TextCnter\">\n            <a\n              class=\"btn btn--pill btn--outline\"\n              href=\"https:\/\/www.ultraconecta.com\/ar\/historias-de-pacientes\/\"\n              >Ver m\u00e1s historias<\/a\n            >\n          <\/div>\n<\/p><\/div>\n<\/article><\/div>\n<\/p><\/div>\n<\/section>\n<p><!-- FEATURES SECTION --><\/p>\n<section class=\"features\">\n<div class=\"container\">\n<h2 class=\"features__heading\">XLH ES UNA ENFERMEDAD HEREDITARIA, PROGRESIVA Y CR\u00d3NICA<\/h2>\n<div class=\"features__grid\">\n      <!-- Feature 1: Hereditaria --><\/p>\n<article class=\"feature\">\n<div class=\"feature__icon\">\n          <img decoding=\"async\" loading=\"lazy\" fetchpriority=\"low\"\n            src=\"https:\/\/www.ultraconecta.com\/ar\/wp-content\/uploads\/X-linked-hypophosphatemia-is-a-hereditary-condition.png\"\n            alt=\"\u00cdconos de caracter\u00edsticas de XLH\"\n            width=\"450\"\n            height=\"550\"\n            class=\"alignnone size-full wp-image-151\"\n          \/>\n        <\/div>\n<h3 class=\"feature__title\">Hereditaria<\/h3>\n<p class=\"feature__text\">\n         XLH es una enfermedad que se transmite de padres a hijos. En el 30% de los casos se presenta por primera vez en personas sin antecedentes familiares.\n        <\/p>\n<p>      <!--  <a\n          class=\"btn btn--pill btn--outline\"\n          href=\"https:\/\/www.ultraconecta.com\/ar\/acerca-de-xlh\/\"\n          >M\u00e1s informaci\u00f3n<br \/>\n          sobre XLH<\/a\n        > --><br \/>\n      <\/article>\n<p>      <!-- Feature 2: Progresiva --><\/p>\n<article class=\"feature\">\n<div class=\"feature__icon\">\n          <img decoding=\"async\" loading=\"lazy\" fetchpriority=\"low\"\n            src=\"https:\/\/www.ultraconecta.com\/ar\/wp-content\/uploads\/Progresiva-1.png\"\n            alt=\"\u00cdconos de caracter\u00edsticas de XLH\"\n            width=\"225\"\n            height=\"191\"\n            class=\"alignnone size-full wp-image-154\"\n          \/>\n        <\/div>\n<h3 class=\"feature__title\">Progresiva<\/h3>\n<p class=\"feature__text\">\n         Nuevos s\u00edntomas pueden aparecer a cualquier edad y agravarse con el paso de los a\u00f1os. Es importante entender la progresi\u00f3n de XLH.\n        <\/p>\n<p>       <!-- <a\n          class=\"btn btn--pill btn--outline\"\n          href=\"https:\/\/www.ultraconecta.com\/ar\/signos-y-sintomas-ninos\/\"\n          >conoc\u00e9 los s\u00edntomas<\/a\n        > --><br \/>\n      <\/article>\n<p>      <!-- Feature 3: Cr\u00f3nica --><\/p>\n<article class=\"feature\">\n<div class=\"feature__icon\">\n          <img decoding=\"async\" loading=\"lazy\" fetchpriority=\"low\"\n            src=\"https:\/\/www.ultraconecta.com\/ar\/wp-content\/uploads\/Cronico-1.png\"\n            alt=\"\u00cdconos de caracter\u00edsticas de XLH\"\n            width=\"225\"\n            height=\"193\"\n            class=\"alignnone size-full wp-image-153\"\n          \/>\n        <\/div>\n<h3 class=\"feature__title\">Cr\u00f3nica<\/h3>\n<p class=\"feature__text text-wrap\">\nLas personas con XLH seguir\u00e1n experimentando s\u00edntomas a lo largo de su vida.\n        <\/p>\n<p>      <!--  <a\n          class=\"btn btn--pill btn--outline\"\n          href=\"https:\/\/www.ultraconecta.com\/ar\/manejo-de-la-enfermedad\/\"\n          >Informaci\u00f3n sobre el manejo de XLH<\/a\n        > --><br \/>\n      <\/article>\n<\/p><\/div>\n<\/p><\/div>\n<\/section>\n<p><!-- CTA BAND \u2014 Centered --><\/p>\n<hr class=\"social-resources__divider\">\n<section class=\"references references-main\">\n<div class=\"container\">\n<div class=\"content-wrap-one\">\n<h2 class=\"references__title\">Referencia:<\/h2>\n<ol class=\"references__list\">\n<li class=\"references__item\">\n          Carpenter TO, et al.\u00a0J Bone Miner Res. 2011 Jul;26(7):1381\u20131388.\n        <\/li>\n<li class=\"references__item\">\n         Haffner D, et al. Nat Rev Nephrol. 2019 Jul;15(7):435-455.\n        <\/li>\n<\/ol><\/div>\n<\/p><\/div>\n<\/section>\n<section class=\"cta-band\">\n<div class=\"container\">\n<div class=\"cta-band__inner\">\n<div class=\"cta-band__icon\" aria-hidden=\"true\">\n        <img decoding=\"async\" loading=\"lazy\"\n          src=\"https:\/\/www.ultraconecta.com\/ar\/wp-content\/uploads\/Importante-1.png\"\n          alt=\"\u00cdconos de caracter\u00edsticas de XLH\"\n          width=\"228\"\n          height=\"195\"\n          class=\"alignnone size-full wp-image-156\"\n        \/>\n      <\/div>\n<div class=\"cta-band__content\">\n<h2 class=\"cta-band__heading\">\n          <span class=\"cta-band__heading-line1\">\u00bfTen\u00e9s sospecha de XLH?<\/span><br \/>\n          <span class=\"cta-band__heading-line2\">Actu\u00e1 a tiempo<\/span><br \/>\n        <\/h2>\n<p class=\"cta-band__text\">\nLa informaci\u00f3n es el primer paso y est\u00e1s en un buen lugar para comenzar. Si algo de lo que le\u00e9s te genera inquietud, confi\u00e1 en tu intuici\u00f3n y consult\u00e1 con un m\u00e9dico para conversar sobre tus dudas y\/o las de tu hijo\n        <\/p>\n<\/p><\/div>\n<\/p><\/div>\n<\/p><\/div>\n<\/section>\n<section class=\"empty-space-section\">\n<\/section>\n","protected":false},"excerpt":{"rendered":"<p>Bastian y su mam\u00e1 Hipofosfatemia ligada al cromosoma X (XLH) XLH es una enfermedad hereditaria, progresiva y cr\u00f3nica que afecta tanto a ni\u00f1os como a adultos. Obten\u00e9 m\u00e1s informaci\u00f3n sobre XLH, sus signos y s\u00edntomas y el manejo de esta enfermedad poco frecuente. m\u00e1s informaci\u00f3n sobre XLH Ver signos y s\u00edntomas &nbsp; Silvia \u201cYo ten\u00eda [&hellip;]<\/p>\n","protected":false},"author":2,"featured_media":0,"parent":0,"menu_order":0,"comment_status":"closed","ping_status":"closed","template":"page-template.php","meta":{"footnotes":""},"class_list":["post-26","page","type-page","status-publish","hentry"],"yoast_head":"<!-- This site is optimized with the Yoast SEO plugin v28.5 - https:\/\/yoast.com\/product\/yoast-seo-wordpress\/ -->\n<title>Informaci\u00f3n sobre Hipofosfatemia Ligada al X | XLH<\/title>\n<meta name=\"description\" content=\"Conoc\u00e9 la Hipofosfatemia Ligada al X (XLH), una enfermedad hereditaria poco frecuente que afecta huesos, m\u00fasculos y dientes. 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