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Indian J Ophthalmol ; 2010 Jul; 58(4): 328-329
Artículo en Inglés | IMSEAR | ID: sea-136082

RESUMEN

An eight-year-old girl, an offspring of a consanguineous marriage presented with multiple anterior stromal geographic corneal opacities in both eyes. She was diagnosed to have superficial variant of granular dystrophy based on the family history, clinical features and mutation of TGF B1 gene. She was treated by alcohol-assisted removal of epithelium followed by mechanical debridement of abnormal deposits. Postoperatively, the cornea in both eyes was clear with no trace of opacity and the patient had an unaided visual acuity of 20/20 partial.


Asunto(s)
Sustitución de Aminoácidos , Antibacterianos/uso terapéutico , Niño , Distrofias Hereditarias de la Córnea/tratamiento farmacológico , Distrofias Hereditarias de la Córnea/genética , Distrofias Hereditarias de la Córnea/cirugía , Desbridamiento/métodos , Femenino , Variación Genética , Homocigoto , Humanos , Masculino , Mutación , Ofloxacino/uso terapéutico , Hermanos , Factor de Crecimiento Transformador beta1/genética , Resultado del Tratamiento , Agudeza Visual
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