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                <text>History and applications of femtosecond lasers -- Femtosecond lasers in corneal surgery -- Principles of femtodynamics -- LASIK with AMO femtosecond lasers: laser settings -- LASIK with AMO femtosecond lasers : LASIK procedure techniques -- LASIK with AMO femtosecond lasers: getting started -- LASIK with AMO femtosecond lasers: troubleshooting -- LASIK with emerging femtosecond laser systems -- Intracorneal ring segments -- IntraLase-enabled keratoplasty -- Future of femtosecond laser technology</text>
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                <text>La Secuencia o Síndrome Moebius es un cuadro congénito heterogéneo que se caracteriza por presentar parálisis facial congénita unilateral o bilateral, simétrica o asimétrica; asociada a la alteración de la motilidad ocular en el plano horizontal. Puede expresarse clínicamente como una parálisis del VI nervio de afectación unilateral o bilateral, como una parálisis de la mirada horizontal, como un síndrome de Duane o como una fibrosis Congénita de los Músculos Extraoculares tipo 1.</text>
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                <text>Radioterapia</text>
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            <description>An account of the resource</description>
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                <text>Un médico siempre busca la mejor opción terapéutica para su paciente. Pero si se trata de un niño que padece un retinoblastoma, es crucial encontrar el camino indicado para darle una solución a su problema, procurando generar los efectos adversos de menor intensidad y sobre todo teniendo como valor máximo a la preservación de la vida.</text>
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                <text>Zelter, Marta</text>
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                <text>Fandiño, Adriana C.</text>
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                <text>Consejo Argentino de Oftalmología</text>
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            <description>A language of the resource</description>
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                <text>spa</text>
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                <text>Frente al diagnóstico de un retinoblastoma en un niño, el primer dilema que debemos resolver es el de la terapéutica que aplicaremos. Esto es: debemos decidir la enucleación frente al tratamiento conservador en uno o ambos ojos. Las metas del tratamiento son, ante todo, salvar la vida, seguidas por la conservación del globo ocular, la preservación de la visión y la prevención de las secuelas. Se mencionan las decisiones a tomar para elegir cada una de las formas de tratamiento.</text>
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                <text>Médico Oftalmólogo, Año 26, nro. 2, mayo de 2013, 16-18.</text>
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                <text>Fandiño, Adriana C.</text>
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                <text>El diagnóstico temprano de Retinoblastoma (RB), el cáncer intraocular más frecuente en la infancia, puede salvar la vida y la visión de un niño.  Sin embargo, la evidencia sugiere que muchos niños en todo el mundo reciben un diagnóstico tardío.</text>
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                <text>Niños</text>
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                <text>Sociedad Argentina de Oftalmología Infantil</text>
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                <text>Revista Argentina de Oftalmología Infantil, marzo de 2020, nro. 1, p. 6-8.</text>
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                <text>Atentos a un gran simulador, el enmascarado… [meduloepitelioma intraocular]</text>
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                <text>Fandiño, Adriana C.</text>
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                <text>Las formas de presentación del meduloepitelioma intraocular son muy variadas. Al inicio puede aparecer como una lesión del cuerpo ciliar que al crecer desarrollara una masa blanco grisácea con quistes intratumorales. La presencia de una membrana ciclítica neoplásica con extensión a la región retrolental es muy característica. Las manifestaciones secundarias como cataratas y glaucoma neovascular pueden estar presentes en hasta 50% y 60% de los pacientes, respectivamente. Estos podrían ser los primeros signos por los cuales, desafortunadamente, alrededor del 50% de los pacientes se someten a cirugía antes de reconocer el tumor oculto. Esta situación, en el caso de tratarse de tumor de estirpe maligna,  podría provocar la invasión extra ocular local orbitaria y enfermedad metastásica, que puede conducir a la muerte</text>
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                <text>Lesiones del cuerpo ciliar</text>
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                <text>Catarata congénita</text>
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                <text>Glaucoma neovascular</text>
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              <elementText elementTextId="84236">
                <text>Glaucoma congénito</text>
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              <elementText elementTextId="84237">
                <text>Glaucoma pediátrico</text>
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                <text>Niños</text>
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              <elementText elementTextId="84239">
                <text>Oftalmología pediátrica</text>
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                <text>Meduloepitelioma del cuerpo ciliar</text>
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              <elementText elementTextId="84241">
                <text>Coloboma de cristalino</text>
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                <text>Casos clínicos</text>
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            <name>Publisher</name>
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                <text>Sociedad Argentina de Oftalmología Infantil</text>
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            <name>Date Created</name>
            <description>Date of creation of the resource.</description>
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                <text>Revista Argentina de Oftalmología Infantil, vol. 1, nro. 2, junio de 2020, p. 12-14.</text>
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                <text>2684-0472</text>
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            <description>A language of the resource</description>
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                <text>Español</text>
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            <description>The nature or genre of the resource</description>
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            <name>Title</name>
            <description>A name given to the resource</description>
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                <text>Un desafío en mi vida.</text>
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            <description>Date of creation of the resource.</description>
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                <text>Año 4, n. 13 (mar. 2011), p. 40-41. Título: Sao News</text>
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                <text>Retinoblastoma</text>
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              <elementText elementTextId="55885">
                <text>Oftalmólogos argentinos</text>
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            <name>Creator</name>
            <description>An entity primarily responsible for making the resource</description>
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                <text>Fandiño, Adriana.</text>
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                <text>Implantes en glaucoma: porqué, cuándo y cómo / Francisco Fantes, Ana Carolina Acosta</text>
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                <text>Visión Pan-Americana; Arlington, Asociación Pan-Americana de Oftalmología, may.-jun. 2004</text>
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                <text>Vol. 3, 2, p.6-9Título: Visión Pan-Americana</text>
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                <text>Glaucoma</text>
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                <text>Molteno</text>
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                <text>Ahmed</text>
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                <text>Baerveldt</text>
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                <text>Lentes de contacto de silicona</text>
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                <text>Lentes de contacto hidrofílicas</text>
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                <text>Fanti, Peter</text>
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              <elementText elementTextId="37347">
                <text>Boca RatonJobson</text>
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                <text>Objetivo. Describir las características clínicas y epidemiológicas de pacientes con toxoplasmosis ocular de presentación atípica atendidos en la sección de Uveítis del Hospital Interzonal General de Agudos Rodolfo Rossi (HIGA Rossi).&#13;
&#13;
Materiales y métodos. Estudio retrospectivo donde se evaluaron historias clínicas de pacientes con diagnóstico clínico de toxoplasmosis ocular, atendidos entre junio de 2023 y junio de 2025. Se identificaron los casos atípicos según criterios clínicos: retinocoroiditis pseudomúltiple, retinitis extensa, papilitis sin foco adyacente, necrosis retiniana aguda o inmunosupresión. Se recopilaron datos clínicos, serológicos y de tratamiento, analizados de forma descriptiva.&#13;
&#13;
Resultados. Se encontraron 23 pacientes con toxoplasmosis ocular, de los cuales 6 (26,1%) presentaron formas atípicas. El motivo de consulta más frecuente fue disminución de agudeza visual. Todos los pacientes presentaron IgG positiva y solo 7 IgM positiva. El tratamiento incluyó antiparasitarios y en casos seleccionados, corticosteroides sistémicos. Las complicaciones observadas fueron catarata, glaucoma, membrana epirretinal y desprendimiento de retina.&#13;
&#13;
Conclusión. En nuestra serie las formas atípicas de toxoplasmosis ocular fueron infrecuentes, pero clínicamente relevantes por su dificultad diagnóstica y tipo de complicaciones. Su identificación requiere un alto índice de sospecha, especialmente en pacientes inmunocomprometidos. El abordaje terapéutico debe ser individualizado y con seguimiento estrecho.</text>
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                <text>Oftalmología Clínica y Experimental, vol. 18, nro. 3, sep. de 2025, p. 287-291</text>
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                <text>Buenos Aires : Sociedad Argentina de Oftalmología,</text>
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                <text>Revista Argentina de Oftalmología Infantil, vol. 1, nro. 3, septiembre de 2020, p. 8-9.</text>
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