Unilateral tuberous sclerosis complex
JCPSP-Journal of the College of Physicians and Surgeons Pakistan. 2004; 14 (10): 628-30
en Inglés
| IMEMR
| ID: emr-66352
ABSTRACT
Tuberous sclerosis is a rare genetic disease of autosomal dominant inheritance, associated with hamartomata formation in several organs and various skin findings. A case of young male is presented here with multiple fibromas on right side of his face, peri-ungual fibromas in right index and middle fingers and right second toe, a small shagreen plaque over right lower back and multiple, ill-defined hypopigmented patches over his right side of the trunk and right buttocks. Fundoscopic examination revealed retinal phacomas on right side. CT-scan brain showed right-sided paraventricular calcification
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Índice:
IMEMR (Mediterraneo Oriental)
Asunto principal:
Piel
/
Esclerosis Tuberosa
/
Fibroma
/
Hamartoma
Límite:
Humanos
/
Masculino
Idioma:
Inglés
Revista:
J. Coll. Physicians Surg. Pak.
Año:
2004
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