گزارش یک مورد اسپاسم شیرخوارگی در زمینه تو بروس اسکلروزیس

ABSTRACT Tuberous Sclerosis(T.S) is an inherited disease (with autosomal dominant trait). It is characterised by different skin manifestations involvement of central nervous system and hamartomas in different organs of the body .Of Course ,about 10% of cases are due to new mutations Presentation of this patient, a 4-month-old male infant with recurrent convulsions cflexor type infantile spasm and hypopigmented skin lesions, is important because T.S. is considered as a rare skin nervous disease (prevalence rate of 1 per 30/000 population). In the past 5 years , until now a similar case has not been reported in Hefdah-Shahriver Hospital of Rasht which is a referal Hospital in Guilan Province. Mean while, the onset of disease with infantile spasms lack of any history of familial marriages and also early appearance of calcification in brain C.T. Scan of the patient at the age of 5 months are all as noteworthy features in the above -mentioned case „since incidence of calcification in CT Scan of these patients is rare before the age of 5 months.