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Symptoms » Ataxia
 

Ataxia

Ataxia: Introduction

Ataxia: Failure of muscular coordination. See free access online books about Ataxia below. See detailed information below for a list of 478 causes of Ataxia, including diseases and drug side effect causes.

» Review Causes of Ataxia: full list

Causes of Ataxia:

The following medical conditions are some of the possible causes of Ataxia. There are likely to be other possible causes, so ask your doctor about your symptoms.

See full list of 478 causes of Ataxia

» Review Causes of Ataxia: full list

Causes of Types of Ataxia:

Review the causes of these more specific types of Ataxia:

Review causes of types of Ataxia in more specific categories:

Review causes of more specific types of Ataxia:

See full list of 7 types for Ataxia

Ataxia: Symptom Checker

Listed below are some combinations of symptoms associated with Ataxia, as listed in our database. Visit the Symptom Checker, to add and remove symptoms and research your condition.

Symptom Checker

Symptom Checker

See full list of 2487 Symptom Checker combinations related to Ataxia

Ataxia Treatments

Review information on Ataxia Treatments.

Causes of General Symptom Types

Research the causes of these more general types of symptom:

Causes of Similar Symptoms to Ataxia

Research the causes of these symptoms that are similar to, or related to, the symptom Ataxia:

Diagnostic Guides for Ataxia

Medical Books Excerpts Read excertps from published book sections related to Ataxia from the following published medical books for more detailed information about Ataxia. Free access (no registration): read all online diagnostic book sections about Ataxia

Medical Books Excerpts
  • ATAXIA
  • "Algorithmic Diagnosis of Symptoms and Signs" (2003)
  • Ataxia
  • "In a Page: Signs and Symptoms" (2004)
  • Ataxia
  • "In A Page: Pediatric Signs and Symptoms" (2007)
  • Ataxia
  • "Handbook of Signs & Symptoms (Third Edition)" (2006)
  • Ataxia
  • "A Pocket Manual of Differential Diagnosis" (1999)
  • Ataxia
  • "Professional Guide to Signs & Symptoms (Fifth Edition)" (2006)
  • Ataxia
  • "The 10-Minute Diagnosis Manual: Symptoms and Signs in the Time-Limited Encounter" (2000)
  • Ataxia
  • "Field Guide to Bedside Diagnosis" (2007)
  • Ataxia
  • "Alarming Signs and Symptoms: Lippincott Manual of Nursing Practice Series" (2007)
  • Ataxia
  • "Signs & Symptoms: A 2-in-1 Reference for Nurses" (2007)
  • Ataxia
  • "The Diagnostic Approach to Symptoms and Signs in Pediatrics" (2006)
  • Ataxia
  • "Nursing: Interpreting Signs and Symptoms" (2007)
 

Copyright notice for book excerpts: Copyright © 2008 Lippincott Williams & Wilkins. All rights reserved.

Ataxia: Research Related Doctors & Specialists

Other ways to find a doctor, or use doctor, physician and specialist online research services:

Stories from Users for Ataxia

Real-life user stories relating to Ataxia:

Videos for Ataxia

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Causes of Ataxia listed in Disease Database:

Other medical conditions listed in the Disease Database as possible causes of Ataxia as a symptom include:

See full list of 478 causes of Ataxia
- (Source - Diseases Database)

Medications or substances causing Ataxia:

The following drugs, medications, substances or toxins are some of the possible causes of Ataxia as a symptom. Always advise your doctor of any medications or treatments you are using, including prescription, over-the-counter, supplements, herbal or alternative treatments.

  • Cytarabine Hydrochloride
  • Cytosar-U
  • AK-Pentolate
  • Cyclopentolate Hydrochloride
  • I-Pentolate
  • Pentolair
  • more causes...»

See full list of 64 medications causing Ataxia

Drug interactions causing Ataxia:

When combined, certain drugs, medications, substances or toxins may react causing Ataxia as a symptom. Always advise your doctor of any medications or treatments you are using, including prescription, over-the-counter, supplements, herbal or alternative treatments.

  • Lithium (Eskalith) and ACE Inhibitor interaction
  • Lithium (Eskalith) and Angiotensin Receptor Blocker (ARBs) interaction
  • Lithium (Eskalith) and COX-2 Inhibitor interaction
  • Lithium (Eskalith) and NSAID interaction
  • Lithium (Eskalith) and Thiazide diuretic interaction
  • Insulin and Phenytoin interaction
  • Clozapine and Carbamazepine interaction
  • Phenytoin and Primidone interaction
  • more interactions...»

See full list of 43 drug interactions causing Ataxia

Definitions of Ataxia:

Ataxia: An inability to coordinate muscle activity during voluntary movement; most often results from disorders of the cerebellum or the posterior columns of the spinal cord; may involve the limbs, head, or trunk. SYN: ataxy, incoordination. [G. a-prov. + taxis, order]
Source: Stedman's Medical Spellchecker, © 2006 Lippincott Williams & Wilkins. All rights reserved.

Awkwardness in motor behavior associated with loss of afferent information from the moving part or with loss of control mechanism of the cerebellum.
- (Source - Diseases Database)

Inability to coordinate voluntary muscle movements; unsteady movements and staggering gait
- (Source - WordNet 2.1)

Awkwardness in motor behavior associated with loss of afferent information from the moving part or with loss of control mechanism of the cerebellum.
- (Source - CRISP)

Organs affected by Ataxia:

The list of organs typically affected by Ataxia may include, but is not limited to:

Detailed list of causes of Ataxia

The list below shows some of the causes of Ataxia mentioned in various sources:

See full list of 478 causes of Ataxia

How Common are these Causes of Ataxia?

This information refers to the general prevalence and incidence of these diseases, not to how likely they are to be the actual cause of Ataxia. Of the 478 causes of Ataxia that we have listed, we have the following prevalence/incidence information:

  • 1 causes are "very common" diseases
  • 2 causes are "common" diseases
  • 5 causes are "uncommon" diseases
  • 12 causes are "rare" diseases
  • 10 causes are "very rare" diseases
  • 456 causes have no prevalence information.

See the analysis of the prevalence of 478 causes of Ataxia

Conditions listing symptoms: Ataxia:

The following list of conditions have 'Ataxia' or similar listed as a symptom in our database. This computer-generated list may be inaccurate or incomplete. Always seek prompt professional medical advice about the cause of any symptom.

Symbols

  • 3- ... ataxic gait
  • 3-alpha-hydroxyisobutyryl-CoA hydrolase deficiency ... ataxia

    A

  • Abetalipoproteinemia ... ataxia
  • Acanthocytosis ... ataxia
  • Aceruloplasminemia ... ataxia
  • Acute Bokhoror ... ataxia
  • Acute Chemical poisoning - Varnish makers' and painters' Naptha ... ataxia
  • Acute Disseminated Encephalomyelitis ... ataxia
  • Acute Pesticide poisoning - xylene ... ataxia
  • Acute VE ... ataxia
  • Acute Viliuisk Encephalitis ... ataxia
  • Acute Viliuisk Encephalomyelitis ... ataxia
  • Acute Vilyuisk Encephalitis ... ataxia
  • Acute Vilyuisk Encephalomyelitis ... ataxia
  • Adult-onset ALD ... ataxia
  • Alexander Syndrome ... ataxia
  • Alpers Syndrome ... ataxia
  • Alpha-ketoglutarate dehydrogenase deficiency ... ataxia
  • Amyloidosis, oculoleptomeningeal ... ataxia
  • Anaemia, sideroblastic, X-linked - ataxia ... ataxia
  • Angelman syndrome ... ataxia
  • Aniridia ataxia renal agenesis psychomotor retardation ... ataxia
  • Apple seed poisoning ... ataxia
  • Arachnoid Cysts ... ataxia
  • Argininosuccinase lyase deficiency, late onset ... ataxia
  • Arizona Bark Scorpion poisoning ... ataxia
  • Arnold-Chiari malformation type 3 ... ataxia
  • Arnold-Chiari malformation type 4 ... ataxia
  • ARTS syndrome ... ataxia
  • Ataxia ... ataxia
  • Ataxia - apraxia - mental retardation, X-linked ... ataxia
  • Ataxia - diabetes - goiter - gonadal insufficiency ... ataxia
  • Ataxia - oculomotor apraxia, type 1 ... ataxia
  • Ataxia deafness reardon type ... ataxia
  • Ataxia spastic congenital miosis ... ataxia
  • Ataxia tapetoretinal degeneration ... ataxia
  • Ataxia with Vitamin E Deficiency ... ataxia
  • Ataxia, spastic with congenital miosis ... gait ataxia
  • Ataxia, spastic, 3, autosomal recessive ... ataxic gait
  • Ataxia-deafness syndrome ... ataxia
  • Ataxia-oculomotor apraxia syndrome ... ataxia

    B

  • Baltic myoclonic epilepsy ... ataxia
  • Bangstad syndrome ... ataxia
  • Basal ganglia calcification, idiopathic 1 ... ataxic gait
  • Basal Ganglia Disease, Adult-Onset ... ataxia
  • Basilar impression primary ... ataxia
  • Baughman syndrome ... ataxia
  • Benign Paroxysmal Positional Vertigo ... Ataxia
  • Bhaskar-Jagannathan syndrome ... ataxia
  • Bickerstaff's brainstem encephalitis ... ataxia
  • Bickerstaff's brainstem encephalitis (BBE) ... ataxia
  • Biotinidase deficiency, late onset ... ataxia
  • Bird-headed dwarfism with progressive ataxia, Insulin-resistant diabetes, goiter and primary gonadal insufficiency ... ataxia
  • Blue-ringed octopus poisoning ... ataxia
  • Bonnemann-Meinecke-Reich syndrome ... ataxia
  • Borud Syndrome ... ataxia
  • Buckeye poisoning ... ataxia

    C

  • California encephalitis ... ataxia
  • Cataract - ataxia - deafness ... ataxia
  • CDG syndrome type 1A ... ataxia
  • CDG syndrome type Ic ... ataxia
  • Celiac disease, susceptibility to 1 ... ataxia
  • Celiac disease, susceptibility to 10 ... ataxia
  • Celiac disease, susceptibility to 11 ... ataxia
  • Celiac disease, susceptibility to 12 ... ataxia
  • Celiac disease, susceptibility to 13 ... ataxia
  • Celiac disease, susceptibility to 2 ... ataxia
  • Celiac disease, susceptibility to 3 ... ataxia
  • Celiac disease, susceptibility to 4 ... ataxia
  • Celiac disease, susceptibility to 5 ... ataxia
  • Celiac disease, susceptibility to 6 ... ataxia
  • Celiac disease, susceptibility to 7 ... ataxia
  • Celiac disease, susceptibility to 8 ... ataxia
  • Celiac disease, susceptibility to 9 ... ataxia
  • Central nervous system lymphoma, primary ... ataxia
  • Central nervous system protozoal infections ... ataxia
  • Cerebellar ataxia - intellectual deficit - optic atrophy - skin abnormalities ... ataxia
  • Cerebellar ataxia type 1, autosomal recessive ... ataxia
  • Cerebellar ataxia, autosomal recessive ... ataxia
  • Cerebellar ataxia, dominant pure ... ataxia
  • Cerebellar ataxia, X-linked ... gait ataxia
  • Cerebellar degeneration, subacute ... gait ataxia, ataxia
  • Cerebellar hypoplasia ... ataxia
  • Cerebellar hypoplasia - endosteal sclerosis ... ataxia
  • Cerebellar hypoplasia - tapetoretinal degeneration ... ataxia
  • Cerebelloolivary atrophy ... ataxia
  • Cerebelloparenchymal autosomal recessive disorder 3 ... ataxia
  • Cerebelloparenchymal disorder V ... ataxia
  • Cerebellum agenesis - hydrocephaly ... ataxia
  • Cerebral Amyloid Angiopathy, Familial ... ataxia
  • Cerebral gigantism - jaw cysts ... ataxia
  • Cerebral sarcoma ... ataxic gait
  • Cerebrorenodigital syndrome ... ataxia
  • Ceroid lipofuscinosis, neuronal 10 ... ataxia
  • Chediak-Higashi like syndrome ... ataxia
  • Chemical poisoning - 2,4,6-Trichlorophenol ... ataxia
  • Chemical poisoning - Acrylamide ... ataxia
  • Chemical poisoning - Aftershave ... ataxia
  • Chemical poisoning - Amitraz ... ataxia
  • Chemical poisoning - Aniline ... ataxia
  • Chemical poisoning - Antifreeze ... ataxia
  • Chemical poisoning - Benzene ... ataxia
  • Chemical poisoning - Gasoline ... ataxia
  • Chemical poisoning - Jet Fuel-4 ... ataxia
  • Chemical poisoning - Mouth Wash ... ataxia
  • Chitayat-Moore-Del Bigio syndrome ... ataxia
  • Chorea familial benign ... gait ataxia
  • Chromosome 15q duplication syndrome ... ataxia
  • Chromosome 15q, trisomy ... Ataxia
  • Chromosome 17, deletion 17q23 q24 ... ataxic gait
  • Chromosome 18q, partial deletion ... ataxia
  • Chromosome 20p, partial duplication ... ataxia
  • Cleft lip palate - deafness - sacral lipoma ... ataxia
  • Cockayne syndrome ... ataxia
  • Coenzyme Q 10 (CoQ10), deficiency ... ataxia
  • Combarros Calleja Leno syndrome ... ataxia
  • Complex 2 mitochondrial respiratory chain deficiency ... ataxia
  • Congenital disorder of glycosylation type 1A ... ataxia
  • Congenital disorder of glycosylation type 1C ... ataxia
  • Congenital disorder of Glycosylation type Ic ... ataxia
  • Congenital Disorders of Glycosylation ... ataxia
  • Congenital Disorders of Glycosylation Type Ia ... ataxia
  • Corneal cerebellar syndrome ... ataxia
  • Craniosynostosis - alopecia - brain defect ... ataxia
  • Cutler Syndrome ... ataxia
  • Cutler-Bass-Romshe syndrome ... ataxia
  • Cystinuria - lysinuria ... ataxia

    D

  • Dandy Walker syndrome recessive form ... ataxia
  • Dandy-Walker - facial hemangioma ... ataxia
  • Dandy-Walker Syndrome ... ataxia
  • De Sanctis-Cacchione syndrome ... ataxia
  • Death Camas poisoning ... ataxia
  • Demyelinating disorder ... Ataxia
  • Diabetes insipidus, diabetes mellitus, optic atrophy ... ataxia
  • Diarrhea chronic with villous atrophy ... ataxia
  • Dinno-Shearer-Weisskopf syndrome ... ataxia
  • Disorder of Cornification 12 (Neutral Lipid Storage Type) ... ataxia
  • DOC 12 (Neutral Lipid Storage Type) ... ataxia
  • Dravet syndrome ... ataxia
  • Dykes-Markes-Harper syndrome ... ataxia
  • Dysequilibrium syndrome ... ataxia

    E

  • Encephalocele anterior ... ataxia
  • Encephalocele frontal ... ataxia
  • Encephaloceles ... ataxia
  • Encephalopathy - intracranial calcification - growth hormone deficiency - microcephaly - retinal degeneration ... ataxia
  • Encephalopathy due to sulphite oxidase deficiency ... ataxia
  • English Ivy poisoning ... ataxia
  • Erythrokeratodermia with ataxia ... gait ataxia
  • Eucalyptus Oil poisoning ... ataxia

    F

  • Fabry's Disease ... ataxia
  • Familial isolated deficiency of vitamin E ... ataxia
  • Feline spongiform encephalopathy ... Ataxia
  • Female carrier ALD ... ataxia
  • Fenton-Wilkinson-Toselano syndrome ... ataxia
  • Friedreich ataxia ... ataxic gait
  • Functioning pancreatic endocrine tumor ... ataxia
  • Furukawa-Takagi-Nakao syndrome ... ataxia

    G

  • Gangliosidosis GM1 type 3 ... gait ataxia
  • Gangliosidosis, generalized GM1 type 2 ... ataxia
  • Gangliosidosis, generalized GM1 type 3 ... gait ataxia
  • Gaucher disease type 2 ... ataxia
  • Glucose transport defect, blood-brain barrier ... ataxia
  • Glutathione Synthetase Deficiency ... cerebellar ataxia in severe forms of the condition
  • Glycine encephalopathy, atypical mild form ... ataxia
  • Golden Chain tree poisoning ... ataxia
  • Granulomatous Angiitis of the Central Nervous System ... ataxia
  • Grass spider poisoning ... ataxia
  • Griscelli disease ... ataxia
  • Griscelli syndrome type I ... ataxia
  • Griscelli syndrome type II ... ataxia

    H

  • Hallervorden-Spatz disease ... ataxia
  • Hartnup Disease ... ataxic gait
  • Heidenhain syndrome ... ataxia
  • Hemangioblastoma ... ataxia
  • Homozygous hypobetalipoproteinemia ... ataxia
  • Hydroxyacyl-coa dehydrogenase, type 2, deficiency ... ataxic gait
  • Hypobetalipoproteinaemia - ataxia - hearing loss ... ataxia
  • Hypotonia, congenital nystagmus, ataxia and abnormal auditory brainstem response ... ataxia

    I

  • Ichythosiform Erythroderma with Leukocyte Vacuolation ... ataxia
  • Immunosuppressive Measles Encephalitis ... ataxia
  • Inborn amino acid metabolism disorder ... ataxia
  • Infant epilepsy with migrant focal crisis ... ataxia
  • Infantile onset spinocerebellar ataxia ... ataxia
  • Infantile polymyoclonus ... ataxia
  • Infantile sialic acid storage disorder ... ataxia
  • Insulinoma ... ataxia

    J

  • Joubert Syndrome ... ataxia
  • Juvenile pilocytic astrocytoma ... ataxia

    K

  • Kearns-Sayre Syndrome ... ataxia
  • Krabbe leukodystrophy ... ataxia

    L

  • Lactic acidosis congenital infantile ... ataxia
  • Lactic Acidosis, Fatal Infantile ... ataxia
  • Lantana poisoning ... ataxia
  • Leukoencephalopathy - metaphyseal chondrodysplasia ... ataxia
  • Lhermitte-McAlpine syndrome ... ataxic gait
  • Lipoamide dehydrogenase deficiency ... ataxia
  • Lithium toxicity ... ataxia
  • Luteinizing hormone releasing hormone, deficiency of, with ataxia ... ataxia

    M

  • Machado-Joseph Disease ... ataxia
  • Macrocytic anemia ... ataxia
  • Macrogyria, pseudobulbar palsy and mental retardation ... ataxia
  • Maple syrup urine disease, type 1A ... ataxia
  • Maple syrup urine disease, type 1B ... ataxia
  • Maple syrup urine disease, type II ... ataxia
  • Maple syrup urine disease, type III ... ataxia
  • Marinesco-Sjogren-like syndrome (MSLS) ... ataxia
  • Mayapple poisoning ... ataxia
  • Measles Encephalitis in Children with Immunosuppression ... ataxia
  • Mediterranean myoclonic epilepsy ... ataxia
  • Medulloblastoma ... ataxic gait
  • Meinecke syndrome ... ataxia
  • Meningoencephalocele ... ataxia
  • Mental retardation - hypocupremia - hypobetalipoproteinemia ... ataxia
  • Mental retardation - macrocephaly - coarse facies - hypotonia ... ataxia
  • Mental retardation - short broad thumbs ... ataxia
  • Mental retardation progressive spasticity ... ataxia
  • Mental retardation progressive spasticity, X-linked ... ataxia
  • Mental retardation, X-linked - seizures - psoriasis ... ataxia
  • Mental retardation, X-linked, with cerebellar hypoplasia and distinctive facial appearance ... ataxia
  • Mercury poisoning - consumption of contaminated fish ... ataxia
  • Mercury poisoning - Folk Remedies ... ataxia
  • Mescal poisoning ... ataxia
  • Metabolic disorders ... Ataxia
  • Metachromatic Leukodystrophy ... ataxia
  • Metastatic insulinoma ... ataxia
  • Mevalonic aciduria ... ataxia
  • Miller Fisher Syndrome ... ataxia
  • Minamata disease ... ataxia
  • Mistletoe poisoning ... ataxia
  • Mitochondrial diseases, clinically indefinite ... ataxia
  • Mitochondrial encephalomyopathy - aminoacidopathy ... ataxia
  • Myoclonus progressive epilepsy of Unverricht and Lundborg ... ataxia
  • Myoclonus-ataxia ... ataxia
  • Myopathy and diabetes mellitus ... ataxia

    N

  • Neuhauser-Daly-Magnelli syndrome ... ataxia
  • Neuroectodermal tumor, primitive ... ataxia
  • Neuroferritinopathy ... ataxia
  • Neuroferritinopathy (adult-onset basal ganglia disease) ... ataxia
  • Neuronal intranuclear hyaline inclusion disease ... ataxia
  • Neuronal intranuclear inclusion disease ... ataxia
  • Niemann-Pick disease ... ataxia

    O

  • Oculodentoosseous dysplasia dominant ... ataxia
  • Olivopontocerebellar Atrophy ... ataxia
  • Olivopontocerebellar atrophy - deafness ... ataxia
  • Ophtalmoplegia - ataxia - hypoacusis ... ataxia
  • Opthalmoplegia ataxia hypoacusis ... ataxia
  • Optic atrophy - ophthalmoplegia - ptosis - deafness - myopathy ... ataxia
  • Optic atrophy, hearing loss and peripheral neuropathy, autosomal recessive ... ataxic gait

    P

  • Partington X-linked mental retardation syndrome ... ataxia
  • Pellagra-like syndrome ... ataxia
  • Pernicious anemia ... ataxia
  • Phenytoin toxicity ... ataxia
  • Phosphoribosylpyrophosphate synthetase superactivity ... ataxia
  • Pili torti - developmental delay - neurological abnormalities ... ataxia
  • Poikilodermatomyositis - mental retardation ... ataxia
  • Posterior column ataxia with retinitis pigmentosa ... ataxia
  • Primary angiitis of the central nervous system ... ataxia
  • Progressive Multifocal Leukoencephalopathy ... ataxia
  • Progressive Rubella Panencephalitis ... ataxia
  • Proximal tubulopathy - diabetes mellitus - cerebellar ataxia ... ataxia
  • Psychogenic Movement Disorders ... ataxia
  • Purine nucleoside phosphorylase deficiency ... ataxia

    R

  • Reardon-Wilson-Cavanagh syndrome ... ataxia
  • Refsum Disease ... ataxia
  • Retinopathy - anaemia- CNS anomalies ... ataxia
  • Rett's syndrome ... gait ataxia
  • Revesz Debuse syndrome ... ataxia
  • Revesz Syndrome ... ataxia
  • Rhombencephalosynapsis ... ataxia
  • Richards-Rundle syndrome ... ataxia
  • Robinow-Unger syndrome ... ataxia
  • Robinson syndrome ... ataxia
  • Rubella panencephalitis ... ataxia

    S

  • SCHAD deficiency ... ataxic gait
  • Schroer-Hammer-Mauldin syndrome ... ataxia
  • Segawa syndrome, autosomal recessive ... gait ataxia
  • Sensory ataxic neuropathy, dysarthria, and ophthalmoparesis ... ataxic gait
  • Sialidosis type 1 ... ataxia
  • Sialidosis type 1 and 3 ... ataxia
  • Sialuria, Finnish type ... ataxia
  • Slowly Progressive Bokhoror ... ataxia
  • Slowly Progressive VE ... ataxia
  • Slowly Progressive Viliuisk Encephalitis ... ataxia
  • Slowly Progressive Viliuisk Encephalomyelitis ... ataxia
  • Slowly Progressive Vilyuisk Encephalitis ... ataxia
  • Slowly Progressive Vilyuisk Encephalomyelitis ... ataxia
  • Spastic paraplegia 23 ... ataxia
  • Spastic paraplegia glaucoma precocious puberty ... ataxia
  • SPG ... ataxia
  • Spinocerebellar Ataxia ... Ataxia
  • Spinocerebellar ataxia - amyotrophy - deafness ... ataxia
  • Spinocerebellar ataxia - dysmorphism ... ataxia
  • Spinocerebellar ataxia 10 ... gait ataxia
  • Spinocerebellar ataxia 11 ... gait ataxia, ataxia
  • Spinocerebellar ataxia 12 ... gait ataxia
  • Spinocerebellar ataxia 13 ... gait ataxia
  • Spinocerebellar ataxia 14 ... gait ataxia
  • Spinocerebellar ataxia 15 ... gait ataxia
  • Spinocerebellar ataxia 16 ... gait ataxia
  • Spinocerebellar ataxia 17 ... gait ataxia, ataxia
  • Spinocerebellar ataxia 18 ... gait ataxia
  • Spinocerebellar ataxia 20 ... gait ataxia, ataxia
  • Spinocerebellar ataxia 21 ... gait ataxia
  • Spinocerebellar ataxia 22 ... gait ataxia
  • Spinocerebellar ataxia 23 ... gait ataxia
  • Spinocerebellar ataxia 25 ... gait ataxia, ataxia
  • Spinocerebellar ataxia 26 ... gait ataxia
  • Spinocerebellar ataxia 27 ... gait ataxia
  • Spinocerebellar ataxia 28 ... gait ataxia
  • Spinocerebellar ataxia 29 ... ataxia
  • Spinocerebellar ataxia 3 ... gait ataxia, ataxia
  • Spinocerebellar ataxia 5 ... gait ataxia
  • Spinocerebellar ataxia 8 ... gait ataxia
  • Spinocerebellar ataxia with axonal neuropathy, type 2 ... ataxia
  • Spinocerebellar ataxia, autosomal recessive 1 ... gait ataxia, ataxia
  • Spinocerebellar ataxia, autosomal recessive 3 ... ataxia
  • Spinocerebellar ataxia, autosomal recessive 4 ... ataxia
  • Spinocerebellar ataxia, autosomal recessive 5 ... ataxia
  • Spinocerebellar ataxia, autosomal recessive 6 ... gait ataxia
  • Spinocerebellar ataxia, autosomal recessive 7 ... gait ataxia
  • Spinocerebellar ataxia, autosomal recessive 9 ... gait ataxia
  • Spinocerebellar ataxia, autosomal recessive, with axonal neuropathy ... gait ataxia, ataxia
  • Spinocerebellar ataxia, Machado-Joseph type I ... gait ataxia
  • Spinocerebellar ataxia, Machado-Joseph type II ... gait ataxia, ataxia
  • Spinocerebellar ataxia, Machado-Joseph type III ... gait ataxia
  • Spinocerebellar ataxia, Machado-Joseph type IV ... gait ataxia
  • Spinocerebellar ataxia, Machado-Joseph type V ... gait ataxia
  • Spinocerebellar ataxia, X-linked, 2 ... ataxia
  • Spinocerebellar ataxia, X-linked, 3 ... ataxia
  • Spinocerebellar ataxia, X-linked, 4 ... ataxia
  • Spinocerebellar ataxia, X-linked, type 4 ... ataxia
  • Spinocerebellar degenerescence, book type ... ataxia
  • Spondyloepimetaphyseal dysplasia, genevieve type ... ataxia
  • SSADH deficiency (succinic semialdehyde dehydrogenase deficiency) ... ataxia
  • Subacute sclerosing leukoencephalitis ... ataxia
  • Subependymoma ... ataxia
  • Susac syndrome ... ataxia

    T

  • Telencephalic leukoencephalopathy ... ataxia
  • Thalamic degeneration symmetrical infantile ... ataxia
  • Thallium poisoning ... Ataxia
  • Thoracic dysplasia - hydrocephalus syndrome ... ataxia
  • Tolterodine toxicity ... ataxia
  • Tome-Brune-Fardeau syndrome ... ataxia
  • Toxic mushrooms - Anticholinergic ... ataxia
  • Toxic mushrooms - Monomethylhydrazine ... ataxia
  • Toxic mushrooms - Psychedelic ... ataxia
  • Tranebjaerg-Svejgaard syndrome ... ataxia
  • Transthyretin amyloidosis ... ataxia
  • Treft-Sanborn-Carey syndrome ... ataxia
  • Triglyceride storage disease with impaired long-chain fatty acid oxidation ... ataxia
  • Trihydroxycholestanoylcoa oxidase isolated deficiency ... ataxia
  • Type 10 17b-hydroxysteroid dehydrogenase deficiency ... ataxic gait

    U

  • Unverricht-Lundborg disease ... ataxia
  • Unverricht-Lundborg syndrome ... ataxia

    V

  • Variant Creutzfeldt-Jakob disease ... Ataxia
  • Vertebral Artery Dissection ... ataxia
  • Vertigo, benign paroxysmal, in childhood ... ataxic gait
  • Vitamin B12 Deficiency ... ataxia

    W

  • Wolfram Syndrome 2 ... ataxia

    X

  • X-linked mental retardation - hypotonia ... ataxia
  • Xeroderma pigmentosum ... ataxia
  • Xeroderma pigmentosum, type 1 ... ataxia
  • Xeroderma pigmentosum, type 2 ... ataxia

    Z

  • Zinc deficiency ... Ataxia

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  • Causes of Ataxia Based on Risk Factors

    This information shows analysis of the list of causes of Ataxia based on whether certain risk factors apply to the patient:

  • Travel - has the patient travelled recently?
  • Diabetes - history of diabetes or family history of diabetes?

    Doctors and specialists: Who should I consult about Ataxia?

    Depending on the seriousness of the onset of Ataxia, you may want to consult one of the following medical professionals.

    Important:In extreme cases, always seek advice from emergency services :

    What are the alternative names for Ataxia:

    Coordination failure, Dyssynergia, Gait abnormality
    - (Source - Diseases Database)

    Classifications of Ataxia:

    Subtypes of Ataxia:

    Gait ataxia (39 causes), Ataxic gait (15 causes)

    Medical Conditions associated with Ataxia:

    Muscle symptoms (4254 causes)

    Symptoms related to Ataxia:

    Muscle symptoms (4254 causes), Tremor (279 causes), Coordination symptoms (351 causes), Movement symptoms (2556 causes), Cerebellar dysfunction, Brain lesions, Nutritional deficiency, Sensory ataxia (4 causes), Imbalance (4 causes), Unsteadiness (595 causes), Gait (452 causes)

    Medical articles on signs and symptoms:

    Doctor-patient articles related to symptoms and diagnosis:

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    See full list of premium articles on symptoms and diagnosis

    Related medical articles from our Disease Center for Ataxia:

    More Ways To Research Medical Signs and Symptoms:


     » Next page: Causes of Ataxia

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