Abstract
The authors represent the clinical case observation of the Schimmelpenning-Feuerstein-Mims syndrome, a congenital dermatological-neurological disease, which includes an organoid epidermal nevus with a wide range of multiple organ dysfunction (neurological, skeletal, cardiovascular, ophthalmological and urological), complicated by the development of rhabdomyosarcoma in a patient. The predominant neurological manifestations of the syndrome are as follows: epilepsy, intellectual and focal disorders. The authors pay specialists’ attention to the complexity of establishing diagnosis and the importance of an interdisciplinary approach in the diagnosis and management in such kind of patients.
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