NEUROCUTANEOUS SYNDROMES: EVALUATION OF CLINICAL AND NEURORADIOLOGICAL FINDINGS

OBJECTIVE: Neurofibromatosis type I (NF1), Tuberous sclerosis complex (TSC) and Sturge-Weber syndrome (SWS) are the most common neurocutaneous syndromes. The purpose of this study is to evaluate clinical neuroradiological manifestations patients diagnosed with NF1, TSC, SWS.MATERIAL AND METHODS: In our clinic, records 15 SWS were retrospectively reviewed between December 2017 May 2019. Clinical detailed.RESULTS: consisting 9 5 1 determined ages days 13,83 years (5 females 10 males). All NF1 had café-au-lait spots. One (11.1%) lisch nodules, one optic glioma, epilepsy, two (22.2%) macrocephaly, hydrocephalus, glioma seven (77.7%) family history established. TSC hypomelanotic macules epilepsy. It was indicated cardiac rhabdomyoma in 3 (60%) patients, angiomyolipoma (20%) patient polycystic kidney patient. showed available facial angioma, glaucoma, pointed UBOs (unknown bright objects) 6 (66.6%) 2 subependymal nodule patients. Brain magnetic resonance imaging all cortical/subcortical tubers nodules. Cortical parenchymal atrophy calcification presented cranial computed tomography SWS.CONCLUSIONS: guidance for diagnosis so that detailed examination perspective on diseases will provide convenience follow-up.