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[Limbal stem cell deficiency associated with KID syndrome, about a case]. / Insuffisance limbique bilatérale associée à un syndrome KID. A propos d'un cas.
Gicquel, J-J; Lami, M-C; Catier, A; Balayre, S; Dighiero, P.
Afiliación
  • Gicquel JJ; Service d'Ophtalmologie, CHU de Poitiers, 2, rue de la Milétrie, BP 577, 86021 Poitiers Cedex.
J Fr Ophtalmol ; 25(10): 1061-4, 2002 Dec.
Article en Fr | MEDLINE | ID: mdl-12527832
We report the case of a 30-year-old woman with KID (keratitis ichthyosis deafness) syndrome consulting for massive corneal neovascularization. She had already undergone two unsuccessful penetrating keratoplasties in her left eye. Visual acuity was limited to no more than light perception because of the opacity and neovascularization of the graft. In the light of this case of limbal cell deficiency, we discuss the ophthalmologic manifestations of KID syndrome as well as its clinical characteristics, physiopathology, and mode of transmission.
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Colección: 01-internacional Base de datos: MEDLINE Asunto principal: Limbo de la Córnea / Enfermedades de la Córnea / Sordera / Ictiosis / Queratitis Tipo de estudio: Risk_factors_studies Límite: Adult / Female / Humans Idioma: Fr Revista: J Fr Ophtalmol Año: 2002 Tipo del documento: Article Pais de publicación: Francia
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Colección: 01-internacional Base de datos: MEDLINE Asunto principal: Limbo de la Córnea / Enfermedades de la Córnea / Sordera / Ictiosis / Queratitis Tipo de estudio: Risk_factors_studies Límite: Adult / Female / Humans Idioma: Fr Revista: J Fr Ophtalmol Año: 2002 Tipo del documento: Article Pais de publicación: Francia