Titlebook: Incidental Findings of the Nervous System; Mehmet Turgut,Fuyou Guo,Sanjay Behari Book 2023 The Editor(s) (if applicable) and The Author(s)

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Agenesis of Corpus Callosumterior to posterior length of this structure. It can be detected in as many as 1–3% of people with poor neurodevelopment. Genetically, 10% of the patients with this impairment have chromosome-related abnormalities, whereas 20–35% have single-gene alterations. The cardinal function of CC is to improv

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Subdural Hematoma have been investigated. Although the pathophysiology of intracranial SDH is still the subject of research, risk factors and the main mechanisms for its acute and chronic forms of intracranial have been researched extensively. In this section, contrary to the expected factors for SDH such as advance

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Dermoid and Epidermoid Cysture of DC is anomalies comprising of hair follicles, sweat glands, sebaceous glands, and lined by stratified squamous epithelium. Conservative treatment is selected in asymptomatic lesions located in deep eloquent area which have been incidentally diagnosticated for intracranial DC or EC. However, s

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Pineal Cystcadian rhythm disorders, and secondary parkinsonism. Pineal gland apoplexy may occur as a rare but serious condition and has a symptomatic course. Although MRI, computed tomography (CT), and transcranial sonography in infants can be used to visualize pineal cysts, some small epiphyseal cysts cannot