Parkinson’s Disease and Cryptogenic Epilepsy
نویسندگان
چکیده
منابع مشابه
Parkinson's Disease and Cryptogenic Epilepsy
Epilepsy is an uncommon comorbidity of Parkinson's disease (PD) and has been considered not directly associated with PD. We present five patients (3 men and 2 women; ages 49-85) who had concomitant PD and cryptogenic epilepsy. Although rare, epilepsy can coexist with PD and their coexistence may influence the progression of PD. While this may be a chance association, an evolving understanding o...
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BACKGROUND Celiac disease (CD) is predominant in women and young people. Atypical, non-enteric symptoms are more common among adults. There is also an association between CD and neurological disorders, especially with cerebellar ataxia, polyneuropathy and epilepsy. AIM To study the frequency of CD in a group of adults with cryptogenic epilepsy. MATERIAL AND METHODS Twenty one patients with ...
متن کاملDiagnosing idiopathic/cryptogenic epilepsy syndromes in infancy.
PURPOSE To determine the characteristics that permit diagnosis of the type of epilepsy beginning in the 1st year of life, and to determine from what age such characteristics are recognisable. PATIENTS From 430 non-selected patients who began having seizures in the 1st year of life and were referred to the neuropaediatric department of Saint Vincent de Paul Hospital, those with epileptic spasm...
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We report three patients with localization-related epilepsy of neonatal onset. They exhibited favourable psychomotor development and had no cerebral lesions on neuroimaging studies despite the presence of intractable partial seizures of neonatal onset. Although rare, some cases of epilepsy of neonatal onset may be cryptogenic, i.e. they belong to neither the symptomatic nor the idiopathic group.
متن کاملCryptogenic gelastic epilepsy: a pediatric case vignette.
Gelastic seizures, characterized by epileptic laughter, are rare and the majority is associated with hypothalamic hamartomas. We report a case with cryptogenic Gelastic seizure (without hypothalamic hamartoma), as the MRI was normal and, EEG and clinical data suggested a focal origin of the seizures.
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ژورنال
عنوان ژورنال: Case Reports in Neurological Medicine
سال: 2016
ISSN: 2090-6668,2090-6676
DOI: 10.1155/2016/3745631