Sandbox kiran3: Difference between revisions

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[[Esophageal motility disorder|Secondary motility disorders]],  
[[Esophageal motility disorder|Secondary motility disorders]],  
[[Shy-Drager syndrome]],  
[[Shy-Drager syndrome]],  
[[Spastic paraplegia 11, autosomal recessive ]],  
[[Hereditary spastic paraplegia|Spastic paraplegia 11, autosomal recessive ]],  
[[Spinal muscular atrophy type I]],  
[[Spinal muscular atrophy type I]],  
[[Spinocerebellar ataxia 17 ]],  
[[Spinocerebellar ataxia|Spinocerebellar ataxia 17 ]],  
[[Spinocerebellar ataxia 22 ]],  
[[Spinocerebellar ataxia|Spinocerebellar ataxia 22 ]],  
[[Spinocerebellar ataxia, autosomal recessive 1 ]],  
[[Spinocerebellar ataxia|Spinocerebellar ataxia, autosomal recessive 1 ]],  
[[Striatonigral degeneration infantile ]],  
[[Striatonigral degeneration infantile ]],  
[[Stroke]],  
[[Stroke]],  

Revision as of 16:38, 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, Congenital myasthenic syndrome 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 gravis, Myoneurogastrointestinal encephalopathy syndrome, Myopathy, Myotonic dystrophy, Neuroferritinopathy, Neurosarcoidosis , osmotic demyelination syndrome paraganglioma, Paraneoplastic limbic encephalitis, Parkinson disease, Peripheral neuropathy, Peripheral tongue paralysis, 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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