Differential (Click to cross reference) acral sensory symptoms Adies pupil ankle reflex, absent areflexia arrhythmia, cardiac ataxia ataxia, cerebellar ataxia, progressive ataxic gait autosomal rcessive spastic ataxia of Charlevoix-Saguenay Babinski sign burning paresthesia cardiomyopathy cerebellar atrophy, primary cerebellar atrophy, secondary Charcot-Marie-Tooth children chorea chromosomal abnormality chromosome 17 Clinical Pathologic Conference(C.P.C.) clubfoot as related to neurologic disease congestive heart failure consanguinity corpus callosum, thinning dexterity, impaired diabetes mellitus distal muscle atrophy distal muscle weakness dysarthria electroencephalogram, inflammatory disease electromyogram falling familial fine motor function, impaired finger nose finger test foot deformity foot drop Friedreich's ataxia gait disorder gene gene mutation genetic counselling genetic neurologic disorders genetic testing hammertoes hand deformity hand weakness hearing loss high arched feet hip pain hyporeflexia imbalance incoordination intrinsic hand muscles, wasting of leg weakness, bilateral middle cerebellar peduncle, lesion middle cerebellar peduncle, lesion, bilateral mitochondrial disease molecular genetics movement disorder MRI, abnormal muscle biopsy muscle weakness, proximal muscular dystrophy muscular dystrophy, cardiovascular changes with myelin protein zero gene myopathy, myofibrillar myotonic discharges nerve conduction studies nerve hypertrophy neurologic disease, diagnoses of neuronopathy, sensory neuropathy neuropathy, hereditary peripheral neuropathy, hypertrophic next-generation sequencing night blindness numbness, extremity nystagmus nystagmus, gaze-evoked orthostatic hypotension paresthesias past pointing pes cavus POLG1 gene pons, lesion of progressive neurologic disorder pupil pupil, dilated and fixed, bilateral respiratory failure review article Romberg's sign scoliosis shoulder, pain in spinocerebellar ataxia steppage gait thalamus, lesion of thalamus, lesion of-bilateral treatment of neurologic disorder tremor tremor, intention trinucleotide repeats visual impairment weakness weakness, progressive weakness, proximal wheelchair winging of scapula

Showing articles 0 to 7 of 7 Slowly rogressive Cerebellar Ataxia in a 55-Year-Old Female Patient JAMA Neurol 80:107-108, Bernaola,M.T.,et al, 2023 Complex Ataxia Neurol 95:136-141, Abkur, T.,et al, 2020 A 52-year-old Woman with Progressive Proximal Weakness Neurol 83:e106-e109, Enduri, S.,et al, 2014 Degenerative Diseases of the Nervous System, Friedreich Ataxia Adams & Victors Principles of Neurology, Chp 39, pg 1102, Ropper, A.H.,et al, 2014 Clinical Reasoning: A 34-Year-Old Woman with Recurrent Bouts of Acral Paresthesias Neurol 74:775-778, Karam,C. &Scelsa,S., 2010 Clinicopath Conf, Charcot-Marie-Tooth Disease Type 2, with Aides Pupil and a Mutation in MPZ Gene NEJM 354:2584-2592, Case 18-2006, 2006 Charcot-Marie-Tooth Disease and Related Inherited Neuropathies Medicine 75:233-250, Murakami,T.,et al, 1996 Showing articles 0 to 7 of 7