Tuberous sclerosis--a multi system disease.
Indian J Pediatr
;
2008 Jan; 75(1): 77-9
Artículo
en Inglés
| IMSEAR
| ID: sea-84775
ABSTRACT
Tuberous sclerosis is a genetic disease with autosomal dominant inheritance, associated with hamartomas in several organs and various skin findings. A case of a ten year old boy is presented here to highlight the multisystem involvement in tuberous sclerosis. The child had seizures, facial papular naevi and peri-ungual fibromas. MRI revealed cortical tubers, white matter lesions and subependymal nodules. Orbital ultrasound showed retinal hamartoma on the left side. Ultrasound of the abdomen revealed a soft tissue mass at the upper pole of left kidney with a small cyst in right kidney.
Texto completo:
Disponible
Índice:
IMSEAR (Asia Sudoriental)
Asunto principal:
Enfermedades de la Retina
/
Convulsiones
/
Neoplasias Cutáneas
/
Esclerosis Tuberosa
/
Encéfalo
/
Humanos
/
Masculino
/
Niño
/
Diagnóstico Diferencial
/
Cara
Tipo de estudio:
Estudio diagnóstico
Idioma:
Inglés
Revista:
Indian J Pediatr
Año:
2008
Tipo del documento:
Artículo
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