A Case of Bilateral Tuberous Sclerosis
Journal of the Korean Ophthalmological Society
;
: 203-209, 1996.
Artigo
em Coreano
| WPRIM
| ID: wpr-108072
ABSTRACT
Tuberous sclerosis is a rare multisystem syndrome characterized by hamartomatous tumors of the brain, skin, viscera, and eye. The diagnostic triad for this disease, proposed by Vogt, included epilepsy, mental retardation, and adenoma sebaceum. In eyes, retinal hamartomas and optic nerve phacoma are observed over 50% and hypopigmented areas of peripheral retina and iris are often found. We introduce an 18-year old girl with adenoma sebaceum of the face, history of epilepsy and insignificant mental retardation status. She also had a retinal hamartoma in her right eye, optic nerve phacoma in her left eye, shagreen patch on lumbosacral area, angiomyolipoma of both kidneys, periventricular subependymal nodules and calcified cortical nodule of occipital lobe of brain.
Texto completo:
DisponíveL
Índice:
WPRIM (Pacífico Ocidental)
Assunto principal:
Nervo Óptico
/
Retina
/
Retinaldeído
/
Pele
/
Esclerose Tuberosa
/
Vísceras
/
Encéfalo
/
Iris
/
Angiomiolipoma
/
Epilepsia
Limite:
Adolescente
/
Feminino
/
Humanos
Idioma:
Coreano
Revista:
Journal of the Korean Ophthalmological Society
Ano de publicação:
1996
Tipo de documento:
Artigo
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