Differential (Click to cross reference) alternating rapid movement aphasia arm swing, reduced asymptomatic ataxia Babinski sign basal ganglia, infarction bradykinesia brain atrophy CAT scan CAT scan, abnormal cerebellar atrophy, primary cerebral autosomal dominate arteriopathy with subcortical infarction and leukoencephalopathy cerebral cortical atrophy cerebral infarction cerebral infarction, small, deep cerebral infarction, subcortical cerebrovascular accident cerebrovascular accident, familial occurrence cerebrovascular accident, multiple cerebrovascular accident, recurrent chromosome 19 Clinical Pathologic Conference(C.P.C.) cognition cogwheel rigidty complications deep gray nuclei degenerative diseases of CNS dementia developmental milestones, loss of dysarthria dysmetria electroencephalogram, abnormalities of external capsule falling familial fine motor function, impaired fingerprint bodies gene gene mutation genetic neurologic disorders genetic screening granular osmiphilic material headache hemiparesis hyperreflexia inclusion bodies inclusion bodies, eosinophilic cytoplasmic intellectual deficit intellectual deterioration introverted leukoencephalopathy memory, impairment of migraine misdiagnosis MRI MRI, abnormal MRI, diffusion weighted multiple sclerosis multiple sclerosis, differential diagnosis of multiple sclerosis, familial multiple sclerosis, misdiagnosis myoclonus myoclonus, epilepsy negative neurologic disease, diagnoses of neuronal ceroid-lipofuscinosis neuropathology Notch3 gene PAS positive PAS positive material in the brain pregnancy, neurologic complications in prognosis progressive myoclonic epilepsy psychiatric problems in neurologic disorders Red flags review article seizure skin, biopsy slurred speech storage disease of CNS stuttering treatment of neurologic disorder tremor tremor, intention vasculopathy walking, difficulty with wheelchair white matter disease wide based gait

Showing articles 0 to 6 of 6 Progressive cognitive decline, cerebellar ataxia, recurrent myoclonus, and epilepsy Neurol 90:e1827-e1831, Xiao, F.,et al, 2018 Clinicopathologic Conference, Kufs Disease (Autosomal Dominant) Parry Type Neuronal Ceroid Lypofuscinosis NEJM 364:1062-1074, Case 8-2011, 2011 Clinicopath Conf, Cerebral Autosomal Dominant Arteriopathy with Subcortical Infarcts and Leukoencephalopathy (CADASIL) NEJM 360:1656-1665, Case 12-2009, 2009 Diagnostic Value of Ultrastructural Skin Biopsy Studies in CADASIL Neurol 68:1430-1432, Malandrini,A.,et al, 2007 Cerebral Autosomal Dominant Arteriopathy With Subcortical Infarcts & Leukoencephalopathy (CADASIL) UpToDate (www.uptodate.com) Aug 21, Dichgans,M.,et al., 2007 Diagnostic Strategies in CADASIL Neurol 59:1134-1138, Markus,H.S.,et al, 2002 Showing articles 0 to 6 of 6