| Cardiovascular
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Stroke
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| Chemical / poisoning
|
Aftershave, barium sulfate, selenious acid, cone shell poisoning, erythrokeratodermia ataxia, eucalyptus oil poisoning, licorice, herbal agent overdose cleistanthus collinus, opioid intoxication, oriental hornet poisoning , snakebites, sea snake poisoning , white chameleon poisoning
|
| Dermatologic
|
Vitamin E deficiency
|
| Drug Side Effect
|
All-trans retinoic acid, cevimeline, clonidine, fluphenazine, imidazoline, lamotrigine, vincristine,lorazepam, nelarabine, oxazepam, oxcarbazepine, perphenazine, phenothiazine, prochlorperazine, saquinavir, thioridazine, tiagabine, trifluoperazine, venlafaxine, vigabatrin, zaleplon
|
| Ear Nose Throat
|
ARTS syndrome
|
| Endocrine
|
Hypokalemic thyrotoxic periodic paralysis
|
| Environmental
|
No underlying causes
|
| Gastroenterologic
|
Chylomicron retention disease
|
| Genetic
|
Jansen's metaphyseal chondrodysplasia, Lambert-Eaton myasthenic syndrome, leigh's disease, lower motor neuron lesion, marinesco-Sjogren syndrome, NADH CoQ reductase deficiency, McLeod phenotype, mental retardation, x-linked, 94, miller fisher syndrome, mitochondrial encephalomyopathy, lactic acidosis, and stroke-like episodes, multifocal motor neuropathy with conduction block, navajo neurohepatopathy, infantile neuroaxonal dystrophy, neuronal intranuclear hyaline inclusion disease, distal hereditary motor type VII, non-ketotic hyperglycemia, Pena-shokeir syndrome type 2, progressive external opthhalmoplegia, autosomal dominant, 1, Roussy-levy syndrome, Smith-Magenis syndrome, Southwestern athabaskan genetic diseases, spastic tetraplegic -- cerebral palsy, spinal bulbar motor neuropathy, spinal muscular atrophy, spinocerebellar ataxia
|
| Hematologic
|
Tang Hsi Ryu syndrome
|
| Iatrogenic
|
No underlying causes
|
| Infectious Disease
|
Lyme disease, quaternary syphilis, tabes dorsalis
|
| Musculoskeletal / Ortho
|
Adducted thumb syndrome recessive form, arthrogryposis due to muscular dystrophy, becker muscular dystrophy, benign congenital hypotonia, brown-Sequard syndrome, bulimia nervosa, CAMFAK syndrome, cauda equina syndrome, cerebro-Oculo-Facio-Skeletal syndrome, charcot-Marie-Tooth disease, type 2, cockayne syndrome, complex 1 mitochondrial respiratory chain deficiency, congenital myopathy, conus medullaris syndrome, distal hereditary motor type VII, Down's syndrome, Duchenne muscular dystrophy, Dykes-Markes-Harper syndrome, emerinopathy, Erb-goldflam, Fazio Londe syndrome , Gerstmann-Straussler-Scheinker syndrome, Guillain-Barré syndrome, Holmes-Adie syndrome, hyperkalemic periodic paralysis, hypokalemic periodic paralysis, hypokalemic thyrotoxic periodic paralysis, Lambert-Eaton myasthenic syndrome, lower motor neuron lesion, muscular dystrophy, multifocal muscular fibrosis, nervous system injuries due to penetrating neck injury, Infantile neuroaxonal dystrophy, neuronal intranuclear hyaline inclusion disease, paramyotonia congenita, penetrating neck injuries, peripheral nerve and muscle disease, polymyositis, progressive external opthhalmoplegia, rommen-mueller-sybert syndrome, scapuloperoneal amyotrophy, schwartz-jampel syndrome, Smith-Magenis syndrome, spinal cord compression, spinal muscular atrophy, transverse myelitis, Treft-sanborn-carey syndrome, Zellweger syndrome
|
| Neurologic
|
Acute weakness in the emergency department, ARTS syndrome, Brown-sequard syndrome, Bulimia nervosa, CAMFAK syndrome,Cauda equina syndrome, central cord syndromes, cerebellar stroke syndrome, Cerebro-Oculo-Facio-Skeletal syndrome, Charcot-Marie-Tooth disease, type 2, coloboma chorioretinal cerebellar vermis aplasia, conus medullaris syndrome , dorsal cord syndrome, Down's syndrome, Friedreich ataxia, folate deficiency, Gerstmann-Straussler-Scheinker syndrome, hypertrophic neuropathy of dejerine-sottas, infantile axonal neuropathy,Krabbe disease,Marinesco-Sjogren syndrome,neuroacanthocytosis, Miller fisher syndrome, muscular dystrophy, navajo neurohepatopathy, nervous system injuries due to penetrating neck injury, paramyotonia congenita, peripheral nerve and muscle disease, spinal muscular atrophy, pure motor lacunar syndrome, quaternary syphilis, rommen-mueller-sybert syndrome, segmental syndrome, spinal cord compression, spinocerebellar ataxia, stroke, transverse myelitis, vitamin E deficiency, ventral cord syndrome
|
| Nutritional / Metabolic
|
3-methylglutaconic aciduria type 4, congenital disorder of glycosylation, cytochrome c oxidase deficiency, folate deficiency, hypermagnesaemia, hypokalemia, hypokalemic periodic paralysis, Krabbe disease, Leigh syndrome, Mcleod phenotype, NADH CoQ reductase deficiency, mitochondrial acetoacetyl-CoA thiolase deficiency, navajo neurohepatopathy, non-ketotic hyperglycemia, Pena-shokeir syndrome type 2, tabes dorsalis, vitamin E deficiency
|
| Obstetric/Gynecologic
|
No underlying causes
|
| Oncologic
|
No underlying causes
|
| Ophthalmologic
|
Cerebro-Oculo-Facio-Skeletal syndrome, Coloboma chorioretinal cerebellar vermis aplasia, Schwartz-jampel syndrome, Treft-sanborn-carey syndrome, Zellweger syndrome
|
| Overdose / Toxicity
|
No underlying causes
|
| Psychiatric
|
No underlying causes
|
| Pulmonary
|
No underlying causes
|
| Renal / Electrolyte
|
Bartter syndrome, neuroaxonal dystrophy renal tubular acidosis,
|
| Rheum / Immune / Allergy
|
Chediak-Higashi Syndrome, multifocal motor neuropathy with conduction block, severe combined immunodeficiency
|
| Sexual
|
No underlying causes
|
| Trauma
|
No underlying causes
|
| Urologic
|
Conus medullaris syndrome
|
| Miscellaneous
|
Hypothermia, stroke
|