Opsoclonus myoclonus syndrome
... cerebellar ataxia, both truncal and appendicular aphasia (a language disorder in which there is an impairment of speech and of ... acute cerebellar encephalopathy (29-32), encephalitis (33), or ataxia (34), syndrome of rapid irregular movements of eyes and ... Opsoclonic Cerebellopathy Opsoclonus-Myoclonus-Ataxia (OMA) Paraneoplastic Opsoclonus-Myoclonus Ataxia (POMA) "Orphanet: ... Gesundheit B, Smith CR, Gerstle JT, Weitzman SS, Chan HS (September 2004). "Ataxia and secretory diarrhea: two unusual ...
Protoparvovirus
... panleukopenia and congenital cerebellar ataxia in domestic cats. In 1978 a virus from the same species as FPV emerged that was ...
List of diseases (M)
Myoclonic progressive familial epilepsy Myoclonus ataxia Myoclonus cerebellar ataxia deafness Myoclonus epilepsy partial ... unusual facies Mumps Münchausen syndrome Münchausen syndrome by proxy Muscle-eye-brain syndrome Muscular atrophy ataxia ... Marfanoid hypermobility Marfanoid mental retardation syndrome autosomal Marginal glioneuronal heterotopia Marie type ataxia ...
Muscular atrophy-ataxia-retinitis pigmentosa-diabetes mellitus syndrome
... cerebellar ataxia, reduced sense of touch, retinal degeneration, and diabetes mellitus beginning in late childhood-early ... Muscular atrophy-ataxia-retinitis pigmentosa-diabetes mellitus syndrome, also known as Kurukawa-Takagi-Nakao syndrome is a very ... "Orphanet: Muscular atrophy ataxia retinitis pigmentosa diabetes mellitus syndrome". www.orpha.net. Retrieved 2022-06-03. "OMIM ... It has been described in 10 members from a large 4-generation Japanese family (1986). "Muscular atrophy ataxia retinitis ...
List of pollution-related diseases
Cardiovascular disease Chronic kidney disease Neurobehavioral impairment Acrodynia Arthritis Cerebellar ataxia Dysarthria ...
List of MeSH codes (C23)
... ataxia MeSH C23.888.592.350.090.200 - cerebellar ataxia MeSH C23.888.592.350.090.600 - gait ataxia MeSH C23.888.592.350.110 - ... gait ataxia MeSH C23.888.592.544 - meningism MeSH C23.888.592.604 - neurobehavioral manifestations MeSH C23.888.592.604.080 - ...
Truncal ataxia
... is caused by midline damage to the cerebellar vermis. There are at least 34 conditions that cause truncal ataxia ... Truncal ataxia is different from appendicular ataxia. Appendicular ataxia affects the movements of the arms and legs. It is ... Alcohol intoxication Cerebral infarction Cerebral hemorrhage Cerebellar ataxia Multiple sclerosis Friedreich's ataxia Drugs ... Truncal ataxia (or trunk ataxia) is a wide-based "drunken sailor" gait characterised by uncertain starts and stops, lateral ...
Kynurenine pathway
... cerebellar ataxia, developmental retardation, coma, renal tubular dysfunction, renal or metabolic acidosis, and even death. The ...
Knuckle-walking
... hands and fully extended legs due to a recessive genetic mutation that causes a nonprogressive congenital cerebellar ataxia ...
Kjer's optic neuropathy
... cerebellar ataxia, spastic paraparesis, myopathy. Dominant optic atrophy is inherited in an autosomal dominant manner. That is ...
Focal neurologic signs
... cerebellar ataxia a gait with a broad base; the patient falters to the side of the lesion (ataxia) inability to coordinate fine ... loss of olfactory functions loss of decision-making ability Cerebellar signs usually involve balance and coordination, and may ...
Guy Cheron
Hz oscillation in the cerebellum of different mouse models presenting neurological diseases ranging from cerebellar ataxia, ... "Cerebellar contribution to visuo-attentional alpha rhythm: insights from weightlessness". {{cite journal}}: Cite journal ... "Inactivation of Calcium-Binding Protein Genes Induces 160 Hz Oscillations in the Cerebellar Cortex of Alert Mice" (PDF). ... "Purkinje cell BKchannel ablation induces abnormal rhythm in deep cerebellar nuclei and prevents Ltd". Scientific Reports. 8 (1 ...
Megalencephalic leukoencephalopathy with subcortical cysts
... progressive and early-onset cerebellar ataxia has been noted in many patients Spasticity Patients with MLC often have muscle ... Central Nervous System Megalencephaly The M in MLC stands for "megalencephaly", the enlargement of the brain Ataxia Slow, ...
Niemann-Pick disease, type C
Neurological signs and symptoms include cerebellar ataxia (unsteady walking with uncoordinated limb movements), dysarthria ( ... "N-Acetyl-L-Leucine for Ataxia-Telangiectasia". clinicaltrials.gov. Retrieved 2019-08-01. "IntraBio". Archived from the original ... and Ataxia-Telangiectasia. Future opportunities to develop N-Acetyl-Leucine include Lewy body dementia, amyotrophic lateral ... and ataxia telangiectasia". Trials. 22 (1): 84. doi:10.1186/s13063-020-05009-3. PMC 7821839. PMID 33482890. "IntraBio Receives ...
List of ICD-9 codes 320-389: diseases of the nervous system and sense organs
Friedreich's ataxia 334.1 Hereditary spastic paraplegia 334.2 Primary cerebellar degeneration 334.3 Other cerebellar ataxia ... Cerebellar ataxia in diseases classified elsewhere 334.8 Other 334.9 Unspecified 335 Anterior horn cell disease 335.0 Werdnig- ...
Frameshift mutation
... is one of the nine codon reiteration disorders caused by polyglutamine expansion mutations that include spino-cerebellar ataxia ...
Ubiquitin carboxy-terminal hydrolase L1
... cerebellar ataxia, nystagmus, dorsal column dysfunction, and upper motor neuron dysfunction. Although UCH-L1 protein expression ...
List of MeSH codes (C10)
... ataxia MeSH C10.597.350.090.500 - cerebellar ataxia MeSH C10.597.350.090.500.530 - spinocerebellar ataxias MeSH C10.597.350.090 ... cerebellar diseases MeSH C10.228.140.252.190 - cerebellar ataxia MeSH C10.228.140.252.190.530 - spinocerebellar ataxias MeSH ... friedreich ataxia MeSH C10.228.140.252.700.250 - myoclonic cerebellar dyssynergia MeSH C10.228.140.252.700.650 - ... friedreich ataxia MeSH C10.228.854.787.500 - myoclonic cerebellar dyssynergia MeSH C10.228.854.787.750 - olivopontocerebellar ...
COA7
... ataxia, cerebellar and spinal cord atrophy, leukoencephalopathy, elevated serum creatine kinase levels, ragged-red fibers, and ... Mutations in COA7 have been associated with cytochrome c oxidase deficiency resulting in spinocerebellar ataxia with axonal ... Mutations in COA7 have been associated with spinocerebellar ataxia with axonal neuropathy type 3 and mitochondrial myopathy ... "Mutations in COA7 cause spinocerebellar ataxia with axonal neuropathy". Brain. 141 (6): 1622-1636. doi:10.1093/brain/awy104. ...
List of diseases (B)
... long thumb type Brachydactyly mesomelia mental retardation heart defects Brachydactyly nystagmus cerebellar ataxia ...
Tityus obscurus
... such as cerebellar ataxia, dysdiadochokinesia, dysmetria, dysarthria, dyslalia, nausea and vomiting; some patients presented ... "Acute cerebellar dysfunction with neuromuscular manifestations after scorpionism presumably caused by Tityus obscurus in ... Tityus obscurus has been responsible for acute cerebellar dysfunction, with neuromuscular manifestations in 58 patients in ...
Nystagmus
Other causes of toxicity that may result in nystagmus include: Brain abscess (cerebellar) Cerebellar ataxia Chiari malformation ... Central nervous system disorders such as with a cerebellar problem, the nystagmus can be in any direction including horizontal ... Gold D. "Gaze-evoked and rebound nystagmus in a cerebellar syndrome". Neuro-Ophthalmology Virtual Education Library (NOVEL): ... Multiple sclerosis Stroke Thalamic hemorrhage Trauma Tumor Infantile cerebellar retinal degeneration Non-physiological ...
List of diseases (A)
Aniridia Aniridia absent patella Aniridia ataxia renal agenesis psychomotor retardation Aniridia cerebellar ataxia mental ... Marie's Ataxia telangiectasia Ataxia telangiectasia variant V1 Atelectasis Atelosteogenesis type I Atelosteogenesis, type II ... Astasia-abasia Astasis Asthenia Asthma Astigmatism Astrocytoma Astrovirus infection Asymmetric septal hypertrophy Ataxia Ataxia ... sideroblastic Anemia sideroblastic spinocerebellar ataxia Anencephaly Anencephaly spina bifida X linked Aneurysm Aneurysm, ...
Thiaminase
... thiaminase in it is causing an acute seasonal cerebellar ataxia named African seasonal ataxia or Nigerian seasonal ataxia. In ... entomophagy in seasonal ataxia patients in Nigeria". J. Nutr. 130: 1625-28. Vetter J (2010). "Toxicological and Medicinal ... placebo-controlled study of the efficacy of thiamine hydrochloride in a seasonal ataxia in Nigerians". Neurology. 44 (3 Pt 1): ...
DDK
... a type of cerebellar ataxia In molecular biology, Cdc7/Dbf4 kinase, or Dbf4-dependent kinase, - protein kinase required for ...
Alcohol-related dementia
... as well as the cerebellum that controls coordination thereby leading to the development of cerebellar ataxia. These patients ... Neuroimaging evidence of cerebellar atrophy, especially in the vermis. C. The following clinical features cast doubt on the ... Ataxia or peripheral sensory polyneuropathy (not attributed to other causes). Beyond 60 days of abstinence, the cognitive ... the presence of focal neurologic signs or symptoms (except ataxia or peripheral sensory polyneuropathy). Neuroimaging evidence ...
List of diseases (P)
... syndrome Pie Torcido Piebald trait neurologic defects Piebaldism Piepkorn-Karp-Hickoc syndrome Pierre Marie cerebellar ataxia ... dystrophy Proximal myotonic myopathy Proximal spinal muscular atrophy Proximal tubulopathy diabetes mellitus cerebellar ataxia ... virus type 3 antenatal infection Paramyotonia congenita of von Eulenburg Paramyotonia congenita Paraneoplastic cerebellar ... Pontoneocerebellar Hypoplasia Popliteal pterygium syndrome lethal type Popliteal pterygium syndrome Porencephaly cerebellar ...
Emmanuel Mignot
Sjögren
... a syndrome consisting of cerebellar ataxia, mental retardation, congenital cataracts Rabén & Sjögren, a book publishing company ...
Canvas (disambiguation)
American vehicle subscription company Cerebellar ataxia, neuropathy, vestibular areflexia syndrome, a neurological disorder ...