A Case of Tuberous Sclerosis
Journal of the Korean Ophthalmological Society
;
: 355-360, 1995.
Artículo
en Coreano
| WPRIM
| ID: wpr-215870
ABSTRACT
Tuberous sclerosis is a heredofamilial disease associated with the diagnostic triad of epilepsy, mental retardation, and skin lesions, adenoma sebaceum. Retinal hamartomas are the most common ocular abnormalities in patients with tuberous sclerosis and are classified as three types 1) large whitish calcified nodular masses, 2) flat transluscent noncalcified smooth tumors, and 3) intermediate type. We introduce a case on 22 year-old male of tuberous sclerosis who was manifested by epilepsy, adenoma sebaceum without mental retardation. And he was characterized by multiple flat transluscent noncalcified type of retinal astrocytic hamartoma accompanied by Shagreen patch, sclerotic calcification in skull and angiomyolipoma on both kidneys.
Texto completo:
Disponible
Índice:
WPRIM (Pacífico Occidental)
Asunto principal:
Retinaldehído
/
Piel
/
Cráneo
/
Esclerosis Tuberosa
/
Angiomiolipoma
/
Epilepsia
/
Hamartoma
/
Riñón
/
Discapacidad Intelectual
Límite:
Humanos
/
Masculino
Idioma:
Coreano
Revista:
Journal of the Korean Ophthalmological Society
Año:
1995
Tipo del documento:
Artículo
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