Ataxia: Difference between revisions
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==Overview== | |||
'''Ataxia''' (from Greek ''α-'' [used as a negative prefix] + ''-τάξις'' [order], meaning "lack of order") is a [[neurology|neurological]] sign and symptom consisting of gross incoordination of [[muscle]] movements. <ref>{{Dorlands|a_69|12166205}}</ref> Ataxia is an aspecific clinical manifestation implying dysfunction of parts of the [[nervous system]] that coordinate movement, such as the [[cerebellum]]. Several possible causes exist for these patterns of neurological dysfunction. The term "dystaxia" is rarely used as a synonym. | '''Ataxia''' (from Greek ''α-'' [used as a negative prefix] + ''-τάξις'' [order], meaning "lack of order") is a [[neurology|neurological]] sign and symptom consisting of gross incoordination of [[muscle]] movements. <ref>{{Dorlands|a_69|12166205}}</ref> Ataxia is an aspecific clinical manifestation implying dysfunction of parts of the [[nervous system]] that coordinate movement, such as the [[cerebellum]]. Several possible causes exist for these patterns of neurological dysfunction. The term "dystaxia" is rarely used as a synonym. | ||
Revision as of 15:04, 16 April 2010
Ataxia | |
ICD-10 | R27.0 |
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ICD-9 | 781.3 |
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Overview
Ataxia (from Greek α- [used as a negative prefix] + -τάξις [order], meaning "lack of order") is a neurological sign and symptom consisting of gross incoordination of muscle movements. [1] Ataxia is an aspecific clinical manifestation implying dysfunction of parts of the nervous system that coordinate movement, such as the cerebellum. Several possible causes exist for these patterns of neurological dysfunction. The term "dystaxia" is rarely used as a synonym.
The International Ataxia Awareness Day is observed on September 25th each year.[2]
Types of ataxia
Cerebellar ataxia
The term cerebellar ataxia is employed to indicate ataxia due to dysfunction of the cerebellum. This causes a variety of elementary neurological deficits, such as antagonist hypotonia, asynergy, dysmetria, dyschronometria, and dysdiadochokinesia. How and where these abnormalities manifest depend on which cerebellar structures are lesioned, and whether the lesion is bilateral or unilateral. Vestibulo-cerebellar dysfunction presents with postural instability, in which the person tends to separate the feet on standing to gain a wider base, and avoid oscillations (especially posterior-anterior ones); instability is therefore worsened when standing with the feet together (irrespective of whether the eyes are open or closed: this is a negative Romberg's test). Spino-cerebellar dysfunction presents with a wide-based "drunken sailor" gait, characterised by uncertain start and stop, lateral deviations, and unequal steps. Cerebro-cerebellar dysfunction presents with disturbances in carrying out voluntary movements, including intention tremor (coarse trembling, accentuated over the execution of voluntary movements, possibly involving the head and eyes as well as the limbs and torso), peculiar writing abnormalities (large, unequal letters, irregular underlining), and a peculiar pattern of dysarthria (slurred speech, sometimes characterised by explosive variations in voice intensity despite a regular rhythm).
Sensory ataxia
The term sensory ataxia is employed to indicate ataxia due to loss of proprioception (sensitivity to joint and body part position), which generally depends on dysfunction of the dorsal columns of the spinal cord, since they carry proprioceptive information up to the brain; in some cases, the cause may instead be dysfunction of the various brain parts that receive that information, including the cerebellum, thalamus, and parietal lobes. Sensory ataxia presents with an unsteady "stomping" gait with heavy heel strikes, as well as postural instability that is characteristically worsened when the lack of proprioceptive input cannot be compensated by visual input, such as in poorly lit environments. Doctors can evidence this during physical examination by having the patient stand with his / her feet together and eyes shut, which will cause the patient's instability to markedly worsen, producing wide oscillations and possibly a fall (this is called a positive Romberg's test). Worsening of the finger-pointing test with the eyes closed is another feature of sensory ataxia. Also, when the patient is standing with arms and hands extended toward the examiner, if the eyes are closed, the patient's finger will tend to "fall down" and be restored to the horizontal extended position by sudden extensor contractions ("ataxic hand").
Vestibular ataxia
The term vestibular ataxia is employed to indicate ataxia due to dysfunction of the vestibular system, which in acute and unilateral cases is associated with prominent vertigo, nausea and vomiting. In slow-onset, chronic bilateral cases of vestibular dysfunction, these characteristic manifestations may be absent, and dysequilibrium may be the sole presentation.
Complete Differential Diagnosis of Ataxia
- Acanthocytosis
- Acoustic neurinoma
- Alcoholism
- Alpha-beta lipoproteinemia
- Arnold-Chiari Malformation
- Arteriosclerosis
- Ataxia-teleangiectasia
- Basilar impression / vertebral-basilar artery ischemia
- Brainstem or cortical lesions
- Cerebellar abscess
- Cerebellar cortex atrophy
- Cerebellar heredoataxia
- Chickenpox
- Circulation disorders in area of brain stem
- Cirrhosis
- Diabetic neuropathy
- Encephalitis
- Epiphyseal tumor
- Familial periodic ataxia
- Fisher's Syndrome
- Fredreich's Ataxia
- Frontal lobe lesion
- GALOP Syndrome (gait disorder, autoantibodies, late age onset, polyneuropathy)
- GM2-gangliosidoses
- Hartnup Syndrome
- Hemorrhage
- Hereditary spastic paraparesis
- HIV infection
- Hypothyroidism
- Hysterical gaits
- Infection
- Inherited neuropathies
- Intoxication
- Malabsorption
- Mann Syndrome
- Marinescu-Garland Syndrome
- Measles
- Mitochondrial cytopathy
- Mononeuropathy/radiculopathy affecting the lower extremities
- Morgagni's Syndrome
- Multiple Sclerosis
- Myelopathy
- Myopathy
- Normal pressure hydrocephalus
- Orthopedic issues affecting the hip, knee, leg, foot, ankle
- Paraneoplastic syndrome
- Parietal lobe lesion
- Parkinsonism
- Peripheral neuropathy
- Polyneuritis
- Smallpox
- Spinal cord compression (and pressure on dorsal nerve roots)
- Spinocerebellar ataxia
- Tabes dorsalis
- Thalamic syndrome
- Thiamine deficiency
- Trauma
- Tumor
- Vestibular apparatus diseases
- Vitamin B12 Deficiency
- Wernicke's Encephalopathy
- Westphal's Disease
- Wilson's Disease
Complete Differential Diagnosis of the Causes of Ataxia
(By organ system)
Cardiovascular |
Arteriosclerosis, Circulation disorders in area of brain stem, Morgagni's Syndrome, |
Chemical / poisoning | No underlying causes |
Dermatologic | No underlying causes |
Drug Side Effect | |
Ear Nose Throat | No underlying causes |
Endocrine | |
Environmental | No underlying causes |
Gastroenterologic | |
Genetic |
Familial periodic ataxia, Fredreich's Ataxia, Hartnup Syndrome, Hereditary spastic paraparesis, Inherited neuropathies, |
Hematologic | |
Iatrogenic | No underlying causes |
Infectious Disease | |
Musculoskeletal / Ortho | |
Neurologic |
Acoustic neurinoma, Arnold-Chiari Malformation, Cerebellar abscess, Cerebellar cortex atrophy, Cerebellar heredoataxia, Encephalitis, GALOP Syndrome (gait disorder, autoantibodies, late age onset, polyneuropathy), Multiple Sclerosis, Normal pressure hydrocephalus, Parkinsonism, Peripheral neuropathy, Polyneuritis, Spinal cord compression(and pressure on dorsal nerve roots), Tabes dorsalis, Wernicke's Encephalopathy, |
Nutritional / Metabolic |
Alcohol, Alpha-beta lipoproteinemia, GM2-gangliosidoses, Thiamine deficiency, Wilson's Disease, |
Obstetric/Gynecologic | No underlying causes |
Oncologic |
Epiphyseal tumor, Paraneoplastic syndrome, |
Opthalmologic | No underlying causes |
Overdose / Toxicity | |
Psychiatric | No underlying causes |
Pulmonary | No underlying causes |
Renal / Electrolyte | No underlying causes |
Rheum / Immune / Allergy | |
Sexual | No underlying causes |
Trauma |
Brainstem or cortical lesions, Frontal lobelesion, Mann Syndrome, Parietal lobelesion, |
Urologic | No underlying causes |
Miscellaneous | Mitochondrial cytopathy, |
Causes of ataxia
The three types of ataxia have overlapping causes, and can therefore either coexist or occurr in isolation.
Focal lesions
Any type of focal lesion of the central nervous system (such as stroke, brain tumour, multiple sclerosis will cause the type of ataxia corresponding to the site of the lesion: cerebellar if in the cerebellum, sensory if in the dorsal spinal cord (and rarely in the thalamus or parietal lobe), vestibular if in the vestibular system (including the vestibular areas of the cerebral cortex).
Exogenous substances
Exogenous substances that cause ataxia mainly do so because they have a depressant effect on central nervous system function. The most common example is ethanol, which is capable of causing overlapping cerebellar and vestibular ataxia. Other examples include both prescription drugs (e.g. most antiepileptic drugs have cerebellar ataxia as a possible unwanted effect) and recreational drugs (e.g. ketamine, PCP).
Vitamin B12 deficiency
Vitamin B12 deficiency may cause, among several neurological abnormalities, overlapping cerebellar and sensory ataxia.
Causes of isolated sensory ataxia
Peripheral neuropathies may cause generalised or localised sensory ataxia (e.g. a limb only) depending on the extent of the neuropathic involvement. Spinal disorders of various types may cause sensory ataxia from the lesioned level below, when they involve the dorsal columns.
Non-hereditary cerebellar degeneration
Non-hereditary causes of cerebellar degeneration include chronic ethanol abuse, paraneoplastic cerebellar degeneration, high altitude cerebral oedema, coeliac disease, and normal pressure hydrocephalus.
Hereditary ataxias
Ataxia may depend on hereditary disorders consisting of degeneration of the cerebellum and/or of the spine; most cases feature both to some extent, and therefore present with overlapping cerebellar and sensory ataxia, even though one is often more evident than the other. Hereditary disorders causing ataxia include autosomal dominant ones such as spinocerebellar ataxia, episodic ataxia, and dentatorubropallidoluysian atrophy, as well as autosomal recessive disorders such as Friedreich's ataxia (sensory and cerebellar, with the former predominating), ataxia-telangiectasia (sensory and cerebellar, with the latter predominating), and abetalipoproteinaemia. An example of X-linked ataxic condition is the rare fragile X-associated tremor/ataxia syndrome.
Treatment
There is no specific treatment for ataxia as such, altough there may be for the underlying cause. The disability of ataxia may be reduced by physical therapy, including exercises, along with leg braces or shoe splints, if foot alignment has been affected; a cane or walker is often used in the effort to prevent falls.
References
- ↑ Template:Dorlands
- ↑ "National Ataxia Foundation - International Ataxia Awareness Day". Retrieved 2008-03-25.
External links
- National Institute of Neurological Disorders and Stroke (NINDS)
- National Ataxia Foundation
- Ataxia UK
- International Ataxia Awareness Day
- Ataxia Forums
- Canadian Association of Familial Ataxias – The Claude St-Jean Foundation
- Video from the US Department of Agriculture of a sheep with scrapie
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