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Longer titles found: Cerebellar ataxia, neuropathy, vestibular areflexia syndrome (view), Acute cerebellar ataxia of childhood (view), Spinocerebellar ataxia (view), Post viral cerebellar ataxia (view), Autosomal dominant cerebellar ataxia (view), Autosomal recessive cerebellar ataxia (view), Autosomal recessive cerebellar ataxia type 1 (view), Autosomal dominant cerebellar ataxia, deafness, and narcolepsy (view), Spinocerebellar ataxia type-13 (view), Spinocerebellar ataxia type 6 (view), Spinocerebellar ataxia type 1 (view)

searching for Cerebellar ataxia 89 found (216 total)

alternate case: cerebellar ataxia

Ramsay Hunt syndrome (315 words) [view diff] no match in snippet view article find links to article

Three different neurological syndromes carry the name of Ramsay Hunt syndrome. Their only connection is that they were all first documented by the famous

VLDLR-associated cerebellar hypoplasia (224 words) [view diff] no match in snippet view article find links to article

VLDLR-associated cerebellar hypoplasia (VLDLRCH) is a rare autosomal recessive condition caused by a disruption of the VLDLR gene. First described as a

Pierre Marie (1,042 words) [view diff] exact match in snippet view article find links to article

hereditary disease of the nervous system, with cerebellar ataxia. "Marie-Foix-Alajouanine syndrome": cerebellar ataxia of the cerebellum in the elderly; usually

Dysequilibrium syndrome (119 words) [view diff] exact match in snippet view article find links to article

may refer to: Cerebellar ataxia, mental retardation, and dysequilibrium syndrome 1 (CAMRQ1), an autosomal recessive cerebellar ataxia associated with

Ulas family (526 words) [view diff] exact match in snippet view article find links to article

The affected siblings have a form of non-progressive congenital cerebellar ataxia. The brain impairments include cerebellar hypoplasia, mild cerebral

CAPOS syndrome (544 words) [view diff] exact match in snippet view article find links to article

present within the body. Usually, individuals with this condition have cerebellar ataxia, areflexia, high-arched feet, optic nerve wasting/degeneration, sensorineural

Paraneoplastic cerebellar degeneration (822 words) [view diff] exact match in snippet view article find links to article

period that can last for months to years. Therefore, newly developing cerebellar ataxia should always prompt proper diagnostic measures to exclude PCD. Tumor

PLEKHG4 (641 words) [view diff] exact match in snippet view article find links to article

(PLEKHG4) gene on chromosome 16q22.1 are not a common genetic cause of cerebellar ataxia in a European population". J Hum Genet. 51 (4): 363–7. doi:10.1007/s10038-006-0372-y

Bhaskar–Jagannathan syndrome (206 words) [view diff] exact match in snippet view article find links to article

conditions are arachnodactyly, aminoaciduria, congenital cataracts, cerebellar ataxia, and delayed developmental milestones. Bhaskar–Jagannathan has symptoms

HERC1 (1,524 words) [view diff] exact match in snippet view article find links to article

pyramidal neurons. Herc1-tbl mutant mice are also characterized by cerebellar ataxia, an unstable gait, and a limb-flexion reflex triggered by tail lifting

Ataxia-pancytopenia syndrome (149 words) [view diff] exact match in snippet view article find links to article

Ataxia-pancytopenia syndrome is a rare autosomal dominant disorder characterized by cerebellar ataxia, peripheral neuropathies, pancytopenia and a predilection to myelodysplastic

International Cooperative Ataxia Rating Scale (378 words) [view diff] exact match in snippet view article find links to article

the goal of standardizing the quantification of impairment due to cerebellar ataxia. The scale is scored out of 100 with 19 items and 4 subscales of postural

Synaptopathy (741 words) [view diff] exact match in snippet view article find links to article

Immune-mediated cerebellar ataxias represent a group of disorders causing cerebellar ataxia induced by a dysfunction of synapses. Increasing knowledge of the

Astasis (1,756 words) [view diff] exact match in snippet view article find links to article

coordination resulting in this deficit. The disturbance differs from cerebellar ataxia in that with astasis the gait can be relatively normal, with balance

GRID2 (2,147 words) [view diff] exact match in snippet view article find links to article

involvement whereas a homozygous biallelic deletion leads to a syndrome of cerebellar ataxia with marked developmental delay, pyramidal tract involvement and tonic

Marinesco–Sjögren syndrome (473 words) [view diff] exact match in snippet view article find links to article

syndrome, is a rare autosomal recessive disorder. The syndrome causes cerebellar ataxia (balance and coordination problems), intellectual disability, congenital

Bromisoval (313 words) [view diff] exact match in snippet view article find links to article

(1998). "Chronic bromvalerylurea intoxication: Dystonic posture and cerebellar ataxia due to nonsteroidal anti-inflammatory drug abuse" (pdf). Internal

Bruns apraxia (793 words) [view diff] exact match in snippet view article find links to article

Bruns apraxia can be distinguished from Parkinsonian ataxia and cerebellar ataxia in a number of ways. Patients typically afflicted with Parkinsonian

AFG3L2 (642 words) [view diff] exact match in snippet view article find links to article

S.; Brusco, A. (2005). "SCA28, a novel form of autosomal dominant cerebellar ataxia on chromosome 18p11.22-q11.2". Brain. 129 (Pt 1): 235–242. doi:10

Motor program (2,629 words) [view diff] exact match in snippet view article find links to article

Bastian, AJ.; Martin, TA.; Keating, JG.; Thach, WT. (Jul 1996). "Cerebellar ataxia: abnormal control of interaction torques across multiple joints".

List of diseases (C) (3,634 words) [view diff] exact match in snippet view article

Cerebellar agenesis Cerebellar ataxia areflexia pes cavus optic atrophy Cerebellar ataxia ectodermal dysplasia Cerebellar ataxia infantile with progressive

Emery–Dreifuss muscular dystrophy (1,459 words) [view diff] case mismatch in snippet view article find links to article

January 1993). "SYNE1 Deficiency". SYNE1-Related Autosomal Recessive Cerebellar Ataxia. GeneReviews. University of Washington, Seattle. Retrieved 10 May

Thiaminase (939 words) [view diff] exact match in snippet view article find links to article

the heat-resistant thiaminase in it is causing an acute seasonal cerebellar ataxia named African seasonal ataxia or Nigerian seasonal ataxia. In 1860–61

Anti-glutamate receptor antibodies (639 words) [view diff] exact match in snippet view article find links to article

Oct;131(1-2):179-85. Shiihara T, Kato M, Konno A, Takahashi Y, Hayasaka K. Acute cerebellar ataxia and consecutive cerebellitis produced by glutamate receptor delta2

Upper limb neurological examination (733 words) [view diff] case mismatch in snippet view article find links to article

PMID 12223260. Diener, HC; Dichgans, J (1992). "Pathophysiology of Cerebellar Ataxia". Movement Disorders. 7 (2): 95–109. doi:10.1002/mds.870070202. PMID 1584245

Cerebrotendineous xanthomatosis (406 words) [view diff] exact match in snippet view article find links to article

normal total cholesterol level; it is characterized by progressive cerebellar ataxia beginning after puberty and by juvenile cataracts, juvenile or infantile

Hypotonia (2,464 words) [view diff] exact match in snippet view article find links to article

Mikhail-Mikhail syndrome, which is characterized by muscular atrophy and cerebellar ataxia which is due to abnormalities in the ATXN1 gene.[citation needed]

SEPP1 (1,121 words) [view diff] exact match in snippet view article find links to article

their SEPP1 homologues (Selenop and SELENOP respectively) may develop cerebellar ataxia phenotypes. SEPP1 and neural precursor cell levels in mouse brains

List of diseases (P) (1,910 words) [view diff] exact match in snippet view article

neurologic defects Piebaldism Piepkorn–Karp–Hickoc syndrome Pierre Marie cerebellar ataxia Pierre Robin sequence Pigmentary retinopathy Pigment dispersion syndrome

ABCB7 (849 words) [view diff] exact match in snippet view article find links to article

PMID 11050011. Maguire A, Hellier K, Hammans S, May A (2002). "X-linked cerebellar ataxia and sideroblastic anaemia associated with a missense mutation in the

Taipei Veterans General Hospital (278 words) [view diff] exact match in snippet view article find links to article

Taiwan (1989) has been pioneering in neurocritical medicine, headache, cerebellar ataxia, dementia, neural regeneration and repair, and epilepsy research and

Leukoencephalopathy with vanishing white matter (2,511 words) [view diff] exact match in snippet view article find links to article

Generally, physicians look for the symptoms in children. Symptoms include cerebellar ataxia, spasticity, optic atrophy, epilepsy, loss of motor functions, irritability

Cerebellar abiotrophy (2,496 words) [view diff] exact match in snippet view article find links to article

Björck G, Everz KE, Hansen HJ, Henricson B (May 1973). "Congenital cerebellar ataxia in the gotland pony breed". Zentralbl Veterinarmed A. 20 (4): 341–354

Scanning speech (301 words) [view diff] case mismatch in snippet view article find links to article

2012-01-04. "Charcot's triad I". whonamedit.com. Retrieved 2012-01-04. Thomas, Huw. "Cerbellar Signs including Cerebellar Ataxia". Retrieved 2012-01-04.

Progressive rubella panencephalitis (392 words) [view diff] exact match in snippet view article find links to article

work 2nd stage: Neurological Changes seizures – sometimes myoclonic cerebellar ataxia spastic weakness retinopathy, optic atrophy frank dementia leading

Behr syndrome (817 words) [view diff] exact match in snippet view article find links to article

Onset : Early childhood Progression: Chronic progressive Clinical: Cerebellar ataxia plus syndrome / Optic Atrophy Plus Syndrome Ocular: Optic atrophy

WD40 repeat (956 words) [view diff] exact match in snippet view article find links to article

TCAB1 55135 WDR80 ATG16L; ATG16B 89849 WDR81 CAMRQ2; PPP1R166 124997 cerebellar ataxia, mental retardation, and dysequilibrium syndrome-2 WDR82 SWD2; MST107;

Posterior cerebral artery (982 words) [view diff] exact match in snippet view article find links to article

subthalamus body or its afferent tracts. Thalamoperforate syndrome: crossed cerebellar ataxia with ipsilateral third nerve palsy (Claude's syndrome): Dentatothalamic

The Family That Walks on All Fours (772 words) [view diff] exact match in snippet view article find links to article

recessive genetic mutation, they have a non-progressive congenital cerebellar ataxia that impairs the balance children normally use to learn to walk bipedally

Ninein (908 words) [view diff] exact match in snippet view article find links to article

centrosome autoantibodies in childhood varicella and post-varicella acute cerebellar ataxia". BMC Pediatrics. 3: 11. doi:10.1186/1471-2431-3-11. PMC 222907. PMID 14503922

List of diseases (B) (1,031 words) [view diff] exact match in snippet view article

mesomelia mental retardation heart defects Brachydactyly nystagmus cerebellar ataxia Brachydactyly preaxial hallux varus Brachydactyly scoliosis carpal

5-Hydroxytryptophan (3,545 words) [view diff] exact match in snippet view article find links to article

also been reported to treat fibromyalgia, myoclonus, migraine, and cerebellar ataxia. However, these clinical findings, as for all therapeutic findings

Kjer's optic neuropathy (1,367 words) [view diff] exact match in snippet view article find links to article

neurological involvement can be observed: peripheral neuropathy, deafness, cerebellar ataxia, spastic paraparesis, myopathy. Dominant optic atrophy is inherited

Ataxin 3 (1,537 words) [view diff] exact match in snippet view article find links to article

Weissenbach J, Cann HM, Agid Y, Brice A (Jan 1995). "The gene for spinal cerebellar ataxia 3 (SCA3) is located in a region of approximately 3 cM on chromosome

MT-ND2 (1,744 words) [view diff] exact match in snippet view article find links to article

disorders and peripheral neuropathy, as well as hypotonia, spasticity and cerebellar ataxia. Roughly half of affected patients die of respiratory or cardiac failure

ADCK3 (559 words) [view diff] exact match in snippet view article find links to article

et al. (2008). "CABC1 gene mutations cause ubiquinone deficiency with cerebellar ataxia and seizures". Am. J. Hum. Genet. 82 (3): 623–30. doi:10.1016/j.ajhg

PLA2G1B (877 words) [view diff] exact match in snippet view article find links to article

"Chromosomal assignment of the second locus for autosomal dominant cerebellar ataxia (SCA2) to chromosome 12q23-24.1". Nat. Genet. 4 (3): 295–9. doi:10

Ceruloplasmin (2,204 words) [view diff] exact match in snippet view article find links to article

may lead to characteristic neurologic signs and symptoms, such as cerebellar ataxia, progressive dementia, and extrapyramidal signs. Excess iron may also

SCARB1 (1,765 words) [view diff] exact match in snippet view article find links to article

Operative Dentistry. 1 (1): 29–35. PMID 1076467. Skre H, Berg K (1974). "Cerebellar ataxia and total albinism: a kindred suggesting pleitotropism or linkage"

PRICKLE1-related progressive myoclonus epilepsy with ataxia (470 words) [view diff] exact match in snippet view article find links to article

Saifi, G. M.; Lupski, J. R. (2005-01-11). "An autosomal recessive cerebellar ataxia syndrome with upward gaze palsy, neuropathy, and seizures". Neurology

Conorenal syndrome (941 words) [view diff] exact match in snippet view article find links to article

1970). "Familial nephropathy associatdd with retinitis pigmentosa, cerebellar ataxia and skeletal abnormalities". Am. J. Med. 49 (4): 556–62. doi:10

Chinese Crested Dog (2,152 words) [view diff] exact match in snippet view article find links to article

Terriers. This is a progressive movement disorder that begins with cerebellar ataxia between 10 and 14 weeks of age. After 6 months of age, affected dogs

Cereblon (1,119 words) [view diff] exact match in snippet view article find links to article

Knaus HG, Wolfer DP, Pedroarena CM, Storm JF, Ruth P (June 2004). "Cerebellar ataxia and Purkinje cell dysfunction caused by Ca2+-activated K+ channel

MT-ND1 (2,022 words) [view diff] exact match in snippet view article find links to article

disorders and peripheral neuropathy, as well as hypotonia, spasticity and cerebellar ataxia. Roughly half of affected individuals die of respiratory or cardiac

Sanger Brown (255 words) [view diff] exact match in snippet view article find links to article

Reserve Corps with rank of first lieutenant. Known for Sanger-Brown cerebellar ataxia. He described it in 1892, it is one of the unusual types collected

William Walton Gooddy (782 words) [view diff] exact match in snippet view article find links to article

P.; Scaravilli, F. (January 1984). "Autosomal dominant late onset cerebellar ataxia with myoclonus, peripheral neuropathy and sensorineural deafness:

Autoimmune GFAP astrocytopathy (645 words) [view diff] exact match in snippet view article find links to article

(choreoathetosis or myoclonus) anti-epileptic drugs (AED)-resistant epilepsy cerebellar ataxia myelitis optic neuritis Some clinical courses could be coincident

Kv1.1 (2,125 words) [view diff] case mismatch in snippet view article find links to article

Episodic Ataxia Type 1, Episodic Ataxia with Myokymia, Hereditary Cerebellar Ataxia with Neuromyotonia Kv1.1+Potassium+Channel at the US National Library

SIL1 (1,454 words) [view diff] exact match in snippet view article find links to article

(December 2005). "Mutations in SIL1 cause Marinesco-Sjögren syndrome, a cerebellar ataxia with cataract and myopathy". Nature Genetics. 37 (12): 1312–4. doi:10

Katherine Safford Harris (915 words) [view diff] exact match in snippet view article find links to article

Rapheal,L.J., Harris, K.S., & Geibel, J.M. (2007). Speech prosody in cerebellar ataxia. "International Journal of Language and Communication Disorders",

Nav1.1 (2,613 words) [view diff] case mismatch in snippet view article find links to article

Missense Mutation in the Sodium Channel Scn8a Is Responsible for Cerebellar Ataxia in the Mouse Mutant jolting. Journal of Neuroscience, 16(19), 5993–5999

Oculomotor apraxia (1,375 words) [view diff] exact match in snippet view article find links to article

onset of symptoms during childhood. It is an autosomal recessive cerebellar ataxia (ARCA) associated with hypoalbuminemia and hypercholesterolemia. Mutations

List of diseases (A) (1,932 words) [view diff] exact match in snippet view article

patella Aniridia ataxia renal agenesis psychomotor retardation Aniridia cerebellar ataxia mental deficiency Aniridia mental retardation syndrome Aniridia ptosis

Familial Danish dementia (954 words) [view diff] exact match in snippet view article find links to article

names FDD Heredopathia ophthalmootoencephalica HOOE ITM2B amyloidosis Cerebellar ataxia, cataract, deafness, and dementia or psychosis Symptoms Cataracts

Aprataxin (1,508 words) [view diff] exact match in snippet view article find links to article

S2CID 29358633. Le Ber I, Moreira MC, Rivaud-Péchoux S, et al. (2003). "Cerebellar ataxia with oculomotor apraxia type 1: clinical and genetic studies". Brain

Mitochondrial disease (3,213 words) [view diff] case mismatch in snippet view article find links to article

Evelyn; Taylor, Robert William; Turnbull, Douglass Matthew (2012). "Cerebellar Ataxia in Patients with Mitochondrial DNA Disease". Journal of Neuropathology

SETX (1,816 words) [view diff] exact match in snippet view article find links to article

Elston J, Hannan MA, et al. (November 2000). "Autosomal recessive cerebellar ataxia with oculomotor apraxia (ataxia-telangiectasia-like syndrome) is linked

Emmanuel Mignot (919 words) [view diff] exact match in snippet view article find links to article

Strom TM, Mignot E. Mutations in DNMT1 cause autosomal dominant cerebellar ataxia, deafness and narcolepsy. Hum Mol Genet. 2012 May 15;21(10):2205-10

Kynurenine pathway (2,249 words) [view diff] exact match in snippet view article find links to article

suffer from tachycardia, irregular breathing, arterial hypotension, cerebellar ataxia, developmental retardation, coma, renal tubular dysfunction, renal

Protoparvovirus (1,555 words) [view diff] exact match in snippet view article find links to article

shown to cause epidemics of enteritis, panleukopenia and congenital cerebellar ataxia in domestic cats. In 1978 a virus from the same species as FPV emerged

PNKP (1,877 words) [view diff] exact match in snippet view article find links to article

Taroni, Franco (2019). "From congenital microcephaly to adult onset cerebellar ataxia: Distinct and overlapping phenotypes in patients with PNKP gene mutations"

Knuckle-walking (2,983 words) [view diff] exact match in snippet view article find links to article

recessive genetic mutation that causes a nonprogressive congenital cerebellar ataxia that impairs the balance needed for bipedality. Not only did they

COACH syndrome (1,972 words) [view diff] exact match in snippet view article find links to article

2753/RUP1061-194008020304377. ISSN 0038-5530. Fogel BL (September 2012). "Childhood cerebellar ataxia". Journal of Child Neurology. 27 (9): 1138–45. doi:10.1177/0883073812448231

TTC19 (1,285 words) [view diff] exact match in snippet view article find links to article

Saitsu, H; Matsumoto, N; Tanaka, F (April 2015). "A Japanese case of cerebellar ataxia, spastic paraparesis and deep sensory impairment associated with a

Opsoclonus myoclonus syndrome (2,290 words) [view diff] exact match in snippet view article find links to article

(brief, involuntary twitching of a muscle or a group of muscles) cerebellar ataxia, both truncal and appendicular aphasia (a language disorder in which

List of diseases (M) (2,464 words) [view diff] exact match in snippet view article

Myoclonic progressive familial epilepsy Myoclonus ataxia Myoclonus cerebellar ataxia deafness Myoclonus epilepsy partial seizure Myoclonus hereditary progressive

Usher syndrome (3,550 words) [view diff] exact match in snippet view article find links to article

"Retinitis pigmentosa combined with congenital deafness with vestibulo-cerebellar ataxia and mental abnormality in a proportion of cases: Clinical and geneto-statistical

Vestibulocerebellar syndrome (1,946 words) [view diff] case mismatch in snippet view article find links to article

"Linkage and Genetic Analysis in Adult Onset Periodic Vestibulo-Cerebellar Ataxia: Report of a New Family." American Journal of Human Genetics 36 (1984):

Frameshift mutation (4,433 words) [view diff] exact match in snippet view article find links to article

disorders caused by polyglutamine expansion mutations that include spino-cerebellar ataxia (SCA) 1, 2, 6, 7 and 3, spinobulbar muscular atrophy and

SURF1 (2,376 words) [view diff] exact match in snippet view article find links to article

polyneuropathy, putaminal and periaqueductal lesions, and late-onset cerebellar ataxia. This disease, when associated with mutations in SURF1, has been found

Rudolph E. Tanzi (4,982 words) [view diff] exact match in snippet view article find links to article

published in the journal, Cell, showing that ATXN1 (encoding the spinal cerebellar ataxia gene product, Ataxin-1) controls production of the amyloid beta protein

Vestibular rehabilitation (2,394 words) [view diff] exact match in snippet view article find links to article

in non-vestibular dizziness are concussions, Parkinson's disease, cerebellar ataxia, normal-pressure hydrocephalus, leukoaraiosis, progressive supranuclear

Glutamate decarboxylase (4,761 words) [view diff] exact match in snippet view article find links to article

of glutamate decarboxylase antibodies in stiff person syndrome and cerebellar ataxia". Orphanet Journal of Rare Diseases. 6 (3): 3. doi:10.1186/1750-1172-6-3

Guy Cheron (1,341 words) [view diff] exact match in snippet view article find links to article

different mouse models presenting neurological diseases ranging from cerebellar ataxia, Angelman syndrome, FAS and Steinert disease. He also actively participate

Phenytoin (4,316 words) [view diff] exact match in snippet view article find links to article

experience vertical nystagmus, double vision, sedation, slurred speech, cerebellar ataxia, and tremor. If phenytoin is stopped abruptly, this may result in

Enteropathy-associated T-cell lymphoma (5,494 words) [view diff] exact match in snippet view article find links to article

other chronic skin conditions, dental enamel defects, gluten-induced cerebellar ataxia, arthritis, and arthralgias. Other gastrointestinal T-cell lymphomas

Childhood immunizations in the United States (7,148 words) [view diff] exact match in snippet view article find links to article

bleeding problems infection or inflammation of the brain (encephalitis, cerebellar ataxia) bacterial infections of the skin and soft tissues in children including

Classification of sleep disorders (3,046 words) [view diff] exact match in snippet view article find links to article

Unspecified hypersomnolence disorder 347.00 G47.419 Autosomal dominant cerebellar ataxia, deafness, and narcolepsy 347.00 G47.419 Autosomal dominant narcolepsy

Pathology of multiple sclerosis (17,122 words) [view diff] exact match in snippet view article find links to article

reveal intrathecal inflammation in progressive MS (SPMS and PPMS) Cerebellar ataxia appears mainly in PPMS and it is related to the pathological changes