Sandbox kiran3: Difference between revisions
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Kiran Singh (talk | contribs) No edit summary |
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[[Brainstem stroke]], | [[Brainstem stroke]], | ||
[[Brain stem tumor|Brainstem tumors]], | [[Brain stem tumor|Brainstem tumors]], | ||
[[ | [[pseudobulbar palsy]], | ||
[[Bulbar palsy]], | [[Bulbar palsy]], | ||
[[Carotid paraganglioma ]], | [[Carotid paraganglioma ]], | ||
| Line 331: | Line 331: | ||
[[Cerebral palsy]], | [[Cerebral palsy]], | ||
[[Cerebrovascular accident]], | [[Cerebrovascular accident]], | ||
[[Cervical osteophytes]], | [[osteophytes|Cervical osteophytes]], | ||
[[Dementia]], | [[Dementia]], | ||
[[Diabetic neuropathy]], | [[Diabetic neuropathy]], | ||
[[Dystonia 12 ]], | [[Dystonia 12 ]], | ||
[[Dystonia | [[Dystonia]], | ||
[[Epileptic encephalopathy, early infantile, 1]], | [[Epileptic encephalopathy, early infantile, 1]], | ||
[[Fosmn syndrome ]], | [[Fosmn syndrome ]], | ||
| Line 344: | Line 344: | ||
[[Infantile striato-thalamic degeneration ]], | [[Infantile striato-thalamic degeneration ]], | ||
[[Lateral funiculus angina]], | [[Lateral funiculus angina]], | ||
[[Lissencephaly, type 1, x- | [[Lissencephaly, type 1, x-linked]], | ||
[[Mass brain lesion]], | [[Mass brain lesion]], | ||
[[Metabolic encephalopathies]], | [[Encephalopathy classification|Metabolic encephalopathies]], | ||
[[Microcephaly brain defect spasticity hypernatremia ]], | [[Microcephaly brain defect spasticity hypernatremia ]], | ||
[[Mitochondrial neurogastrointestinal encephalopathy syndrome]], | [[Mitochondrial neurogastrointestinal encephalopathy syndrome]], | ||
Revision as of 18:46, 18 December 2015
- 10th cranial nerve disorder
- Aberrant subclavian artery
- Abscess
- Achalasia
- Achalasia cardia
- Achalasia, familial esophageal
- Achalasia-addisonian syndrome
- Achromatopsia
- Acoustic neuroma
- Adrenoleukodystrophy
- Aerophagia
- Agranulocytosis
- Alcoholism
- Allergic swelling
- Amyloidosis
- Amyotrophic lateral sclerosis
- Angina tonsillaris
- Anxiety disorders
- Aortic aneurysm
- Arizona bark scorpion poisoning
- Arnold-chiari malformation type 3
- Artemether and lumefantrin
- Aspiration of foreign body
- Autonomic nerve disorders
- Autonomic neuropathy
- Autosomal recessive spastic paraplegia, type 11
- Avellis syndrome
- Babinski–Nageotte syndrome
- Barret's syndrome
- Basal ganglia disease
- Basilar artery insufficiency syndrome
- Behcet's syndrome
- Benign tumors
- Botulinum toxin
- Botulism
- Brainstem stroke
- Brain stem tumor
- Bronchial carcinoma
- Bulbar palsy
- Calcinosis-raynaud's sclerodactyly-telangiectasia syndrome
- Candida esophagitis
- Candidiasis
- Canomad syndrome
- Carcinoma of the vocal tract
- Carotid body tumor
- Carotid paraganglioma
- Cascade stomach
- Caustic esophagitis
- Central pontine myelinosis
- Central vagal nucleus lesion
- Central hypoglossal nerve paralysis
- Cerebellar stroke
- Cerebral palsy
- Cerebrovascular accident
- Cervical osteophytes
- Chagas disease
- Charge syndrome
- Chemical burns
- Chemotherapy
- Chordoma
- Chromosome 1p36 deletion syndrome
- Chromosome 22 ring
- Chromosome 22 trisomy mosaic
- Cobra poisoning
- Congenital bronchogenic cyst
- Connective tissue disease
- Crest syndrome
- Cricopharyngeal spasm
- Crisponi syndrome
- Crohn's disease of the esophagus
- Cushing's syndrome
- Cyclosporine toxicity
- Cytarabine
- Cytomegalovirus
- Cytoplasmic body myopathy
- Dementia
- Dermatomyositis
- Diabetic neuropathy
- Diffuse esophageal spasm
- Diffuse idiopathic skeletal hyperostosis
- Diffuse esophageal spasm
- Diffuse systemic sclerosis
- Diphtheria
- Distal myopathy 2
- Diverticula
- Diverticulum
- Double aortic arch
- Dystonia
- Eagle syndrome
- Elongated styloid process
- Emanuel syndrome
- Enlarged aorta
- Enlarged left atrium
- Eosinophilic esophagitis
- Eosinophilic gastroenteritis
- Epiglottitis
- Epileptic encephalopathy, early infantile, 1
- Esophageal achalasia
- Esophageal atresia
- Esophageal cancer
- Esophageal cyst
- Esophageal diverticulum
- Esophageal leiomyoma
- Esophageal obstruction by a foreign body
- Esophageal pouch
- Esophageal spasm
- Esophageal stricture
- Esophageal web
- Esophageal crohn's disease
- Esophageal moniliasis
- Esophageal sarcoidosis
- Esophageal trauma
- Esophagitis
- Esophagotracheal fistula
- External esophageal compression
- Extreme spinal curvature
- Fluoridated toothpaste
- Food bolus
- Facial Onset Sensory Motor Neuropathy syndrome
- Franek-bocker-kahlen syndrome
- Frontotemporal dementia
- Functional disorders
- Gastric cancer
- Gastric volvulus
- Gastritis
- Gastroesophageal reflux
- Gastroparesis
- Gaucher disease
- Gaucher disease type 2
- Global hystericus
- Globus syndrome
- Goiter
- Graft-versus-host disease
- Guillain-Barré syndrome
- Head trauma
- Herpangina
- Herpes simplex virus
- Hiatal hernia
- Huntington disease
- Huntington's chorea
- Hydroxocobalamin
- Hyperthyroidism
- Hypokalemia
- Hypomagnesemia primary
- Hypophosphatemia
- Hypothyroidism
- Idiopathic human immunodeficiency virus ulcers
- Impaired sensitivity in the larynx
- Inclusion body myositis
- Infantile striato-thalamic degeneration
- Infectious esophagitis
- Intramural pseudodiverticulosis
- Ixabepilone
- Laryngeal cancer
- Laryngeal papillomatosis
- Lateral funiculus angina
- Lead poisoning
- Leiomyoma
- Lhermitte-cornil-quesnel syndrome
- Lissencephaly, type 1, x-linked
- Ludwig's angina
- Lyme disease
- Lymph granulomatosis
- Lymphadenopathy
- Lymphocytic esophagitis
- Malignancy
- Malignant lung cancer
- Mass brain lesion
- Mediastinal mass
- Mediastinitis
- Metabolic encephalopathies
- Microcephaly brain defect spasticity hypernatremia
- Mitochondrial neurogastrointestinal encephalopathy syndrome
- Mitral valve stenosis
- Mononucleosis
- Motor neuron disease
- Mucositis
- Multiple sclerosis
- Multiple system atrophy
- Mumps
- Muscular dystrophy, Duchenne and Becker type
- Myasthenia gravis
- Congenital myasthenic syndrome
- Myoneurogastrointestinal encephalopathy syndrome
- Myopathy
- Myotonic dystrophy
- Nasopharyngeal carcinoma
- Neck cancer
- Nemaline myopathy 1
- Neonatal tetanus
- Neuroferritinopathy
- Neuroleptics
- Neurosarcoidosis
- Nutcracker esophagus
- Oculopharyngeal muscular dystrophy
- Odontoma
- Esophageal cancer
- Esophageal foreign body
- esophageal ring
- Esophageal web
- Esophagitis
- Ondine's curse
- Opitz-frias syndrome
- Oral candidiasis
- Oral cavity tumor
- Oral pharyngeal disorders
- Oral submucous fibrosis
- Oropharyngeal cancer
- Osteophytes
- Palate cancer
- Palatoplegia after damage to the vagal nerve or the accessory nerve
- Pallidopyramidal syndrome
- Paracoccidioidomycosis
- Paraganglioma
- Paraneoplastic limbic encephalitis
- Paraneoplastic syndrome
- Parkinson disease
- Peptic esophagitis
- Peptic stricture
- Pergolide
- Pericarditis
- Peripheral neuropathy
- Peripheral tongue paralysis with lesions of the hypoglossal nerve
- Pharyngeal pouch
- Pharyngitis
- Pharynx cancer
- Pierre Robin syndrome
- Pill esophagitis
- Pleuritis
- Plummer-Vinson syndrome
- Polio
- Poliomyelitis
- Polyradiculitis
- Pontocerebellar hypoplasia type 2a
- Post surgery (laryngeal, esophageal, gastric)
- Post polio syndrome
- Postsurgical muscular or neurogenic
- Primary lateral sclerosis, adult
- Primary motility disorders
- Pseudoachalasia
- Pseudoadrenoleukodystrophy
- Pseudobulbar paralysis
- Pyloric stenosis
- Quinsy
- Rabies
- Radiation esophagitis
- Radiation therapy
- Recent tracheotomy
- Reflux esophagitis
- Retropharyngeal abscess
- Rheumatoid arthritis
- Riedel thyroiditis
- Esophageal web
- Riociguat
- Rumination disorder
- Sarcoidosis
- Sargramostim
- Scarlet fever
- Schatzki ring
- Scleroderma
- [Esophageal motility disorder[|Secondary motility disorders]]
- Sensory ataxic neuropathy, dysarthria, and ophthalmoparesis
- Shy-Drager Syndrome
- Small cell lung cancer
- Spastic paraplegia 11, autosomal recessive
- Spinal muscular atrophy type I
- Spinocerebellar ataxia 17
- Spinocerebellar ataxia 22
- Spinocerebellar ataxia, autosomal recessive 1
- Stevens-Johnson syndrome
- Stomach cancer
- Stomatitis
- Striatonigral degeneration infantile
- Stroke
- Stuve-wiedemann dysplasia
- Subacute granulomatous thyroiditis
- Subacute thyroiditis
- Supraglottic laryngeal cancer
- Syphilis
- Syringobulbia
- Systemic lupus erythematosus
- Systemic sclerosis
- Tardive dyskinesia
- Tetanus
- Throat cancer
- Thyroglossal tract cyst
- Thyroid cancer, anaplastic
- Thyrotoxicosis
- Tiagabine
- Tongue cancer
- Tongue conditions
- Tonsil cancer
- Tonsil disorders
- Tonsillar cancer
- Tonsillar abscess
- Typhoid fever angina
- Ulcer
- Upper oesophageal sphincter dysfunction
- Vagal paraganglioma
- Vascular abnormality
- Vascular ring with right aortic arch
- Vincent's angina
- Wallenberg's syndrome
- Wiedemann–Rautenstrauch syndrome
- Wilson disease
- Zenker's diverticulum
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 , Brainstem stroke, Brainstem tumors, pseudobulbar palsy, Bulbar palsy, Carotid paraganglioma , Central pontine myelinosis, Central vagal nucleus lesion, Central hypoglossal nerve paralysis, Cerebellar stroke, Cerebral palsy, Cerebrovascular accident, Cervical osteophytes, Dementia, Diabetic neuropathy, Dystonia 12 , Dystonia, Epileptic encephalopathy, early infantile, 1, Fosmn syndrome , Guillain-barre syndrome, Head trauma, Huntington disease, Huntington's chorea, Infantile striato-thalamic degeneration , Lateral funiculus angina, 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 , 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, 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, Wallenberg's syndrome ,
Amyotrophic lateral sclerosis,
autonomic neuropathy,
brain stem gliomas,
bulbar palsy,
central pontine myelinolysis,
cerebellar Infarction,
Chagas' disease,
Guillain-Barre syndrome,
lateral medullary syndrome,
multiple sclerosis,
myasthenia gravis,
myotonic dystrophy,
osmotic demyelination syndrome,
paraganglioma,
Parkinson's disease,
pseudobulbar palsy,
pseudodysphagia,
vagus nerve palsy,
Wallenbergs Syndrome
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