Hallervorden-Spatz disease. Clinical-radiological manifestations. Presentation of a case

A case report of an 18-year-old female patient with Hallervorden-Spatz disease, from the age of 4 years, the patient presented with progressive neurological symptoms, consisting of abnormal movements of the upper limbs, dysarthria and mental deterioration. Magnetic resonance imaging showed abnormal iron deposits in the globus pallidus and substantia nigra, confirming the clinical diagnoses