Sandbox kiran3: Difference between revisions

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[[Diabetic neuropathy]],  
[[Diabetic neuropathy]],  
[[Dystonia]],  
[[Dystonia]],  
[[Epileptic encephalopathy, early infantile, 1]],  
[[Ohtahara syndrome|Epileptic encephalopathy, early infantile, 1]],  
[[Fosmn syndrome ]],  
[[Facial Onset Sensory Motor Neuropathy syndrome|Fosmn syndrome ]],  
[[Guillain-barre syndrome]],  
[[Guillain-barre syndrome]],  
[[Head trauma]],  
[[Head trauma]],  
[[Huntington disease]],  
[[Huntington disease]],  
[[Huntington's chorea]],
[[Infantile striato-thalamic degeneration ]],  
[[Infantile striato-thalamic degeneration ]],  
[[Lateral funiculus angina]],
[[Lateral funiculus angina]],

Revision as of 15:31, 21 December 2015


Neurology

10th cranial nerve disorder, Amyotrophic lateral sclerosis, Arnold–Chiari malformation, Ataxia neuropathy spectrum, Autonomic nerve disorders , Autonomic neuropathy, Autosomal recessive spastic paraplegia, type 11, Avellis syndrome, Babinski–Nageotte syndrome, Basal ganglia disease, Basilar artery insufficiency syndrome , Brain stem gliomas Brainstem stroke, Brainstem tumors, pseudobulbar palsy, Bulbar palsy, Carotid paraganglioma , Central pontine myelinosis, Central vagal nucleus lesion, Central hypoglossal nerve paralysis, cerebellar Infarction Cerebellar stroke, Cerebral palsy, Cerebrovascular accident, Cervical osteophytes, Dementia, Diabetic neuropathy, Dystonia, Epileptic encephalopathy, early infantile, 1, Fosmn syndrome , Guillain-barre syndrome, Head trauma, Huntington disease, Infantile striato-thalamic degeneration , Lateral funiculus angina, Lateral medullary syndrome Lissencephaly, type 1, x-linked, Mass brain lesion, Metabolic encephalopathies, Microcephaly brain defect spasticity hypernatremia , Mitochondrial neurogastrointestinal encephalopathy syndrome, Motor neuron disease, Multiple sclerosis, Multiple system atrophy , Muscular dystrophy, duchenne and becker type , Myasthenia gravia, Myasthenic syndrome, congenital, Myoneurogastrointestinal encephalopathy syndrome, Myopathy, Myotonic dystrophy, Neuroferritinopathy, Neurosarcoidosis , osmotic demyelination syndrome paraganglioma, Paraneoplastic limbic encephalitis, Parkinson disease, Peripheral neuropathy, Peripheral tongue paralysis with lesions of the hypoglossal nerve, Polyradiculitis, Pontocerebellar hypoplasia type 2a, Primary lateral sclerosis, adult  , Primary motility disorders, Pseudobulbar paralysis, pseudodysphagia Secondary motility disorders, Shy-Drager syndrome, Spastic paraplegia 11, autosomal recessive , Spinal muscular atrophy type I, Spinocerebellar ataxia 17 , Spinocerebellar ataxia 22 , Spinocerebellar ataxia, autosomal recessive 1 , Striatonigral degeneration infantile , Stroke, Syringobulbia, Tardive dyskinesia, vagus nerve palsy Wallenberg's syndrome ,


















Nissen fundoplication, ,

Oropharyngeal cancer, Ortner's syndrome, palate cancer, palatine tonsil,

post surgery (laryngeal, esophageal, gastric), presbyphagia, pseudoachalasia, quinsy, radiation esophagitis/stricture, retropharyngeal abscess, Schatzki ring, scleroderma, Wilson disease, Zenker's diverticulum

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