A Case of Sjogren-Larsson Syndrome
Journal of the Korean Ophthalmological Society
;
: 1605-1609, 1995.
Artículo
en Coreano
| WPRIM
| ID: wpr-172475
ABSTRACT
The Sjogren-Larsson syndrome is genetically determined syndrome with autosomal recessive inheritence and characterized by the three cardinal signs congenital ichthyosis, spastic di/tetraplegia, and mental retardation. Ocular signs include ectropion, blepharitis, conjunctivitis, keratitis, and macular glistening spot. The authors have experienced a case of Sjogren-Larsson syndrome that showed classical triad and macular glistening spot in a 16 month old boy.
Texto completo:
Disponible
Índice:
WPRIM (Pacífico Occidental)
Asunto principal:
Blefaritis
/
Síndrome de Sjögren-Larsson
/
Conjuntivitis
/
Ectropión
/
Ictiosis
/
Queratitis
/
Discapacidad Intelectual
/
Espasticidad Muscular
Límite:
Humanos
/
Lactante
/
Masculino
Idioma:
Coreano
Revista:
Journal of the Korean Ophthalmological Society
Año:
1995
Tipo del documento:
Artículo
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