| SCA | self-care agency; severe congenital anomaly; sickle-cell anemia; single-camera autostereoscopic [ima... |
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| DSCT | dorsal spinocerebellar tract |
| SCD | scleroderma; service-connected disability; sickle-cell disease; spinocerebellar degeneration; subacu... |
| SDSEM | spinocerebellar degeneration-slow eye movements [syndrome] |
| SpnCbT | spinocerebellar tract |
| SCA1 | Spinocerebellar Ataxia 1 |
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| SCA2 | Spinocerebellar Ataxia Type 2 |
| SCA | Spinocerebellar ataxia |
| SCA-2 | Spinocerebellar ataxia 2 |
| SCA7 | Spinocerebellar ataxia 7 |
| spinocerebellar ataxia | The most common hereditary ataxia, with onset in middle to late childhood, manifested as limb ataxia, nystagmus, kyphoscoliosis, and pes cavus; the major pathological changes are found in the posterior columns of the spinal cord; most often autosomal recessive inheritance. (05 Mar 2000) |
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| anterior spinocerebellar tract | A bundle of fibres originating in the base of the posterior horn and zona intermedia throughout lumbosacral segments of the spinal cord, crossing to the opposite side and ascending in a peripheral position in the ventral half of the lateral funiculus. In its ascent through the rhombencephalon, the tract curves sharply dorsalward along the rostral border of the trigeminal motor nucleus, entering the cerebellum in a caudal direction over the dorsal surface of the superior cerebellar peduncle, and terminating as mossy fibres in the granular layer of the cortex of the cerebellar vermis. The bundle conveys proprioceptive and exteroceptive information largely from the opposite lower extremity. Synonym: tractus spinocerebellaris anterior, Gowers' column, Gowers' tract, ventral spinocerebellar tract. (05 Mar 2000) |
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| ventral spinocerebellar tract | A bundle of fibres originating in the base of the posterior horn and zona intermedia throughout lumbosacral segments of the spinal cord, crossing to the opposite side and ascending in a peripheral position in the ventral half of the lateral funiculus. In its ascent through the rhombencephalon, the tract curves sharply dorsalward along the rostral border of the trigeminal motor nucleus, entering the cerebellum in a caudal direction over the dorsal surface of the superior cerebellar peduncle, and terminating as mossy fibres in the granular layer of the cortex of the cerebellar vermis. The bundle conveys proprioceptive and exteroceptive information largely from the opposite lower extremity. Synonym: tractus spinocerebellaris anterior, Gowers' column, Gowers' tract, ventral spinocerebellar tract. (05 Mar 2000) |
| posterior spinocerebellar tract | A compact bundle of heavily myelinated, thick fibres at the periphery of the dorsal half of the lateral funiculus of the spinal cord, originating in the ipsilateral thoracic nucleus (column of Clarke) and ascending by way of the inferior cerebellar peduncle. Terminals end as mossy fibres in the granular layer of the cortex of the cerebellar vermis. The bundle conveys largely proprioceptive information originating from the annulospiral nerve endings surrounding muscle spindles and from Golgi tendon organs. Synonym: tractus spinocerebellaris posterior, Flechsig's tract. (05 Mar 2000) |
| spinocerebellar degeneration | An autosomal recessive inherited disorder that leads to the progressive dysfunction of the cerebellum, spinal cord and peripheral nerves. Symptoms usually begin in childhood before puberty and consist of an unsteady gait (ataxia), slurred speech (dysarthria) and jerky eye movements (nystagmus). Other findings include kyphoscoliosis, hammer toe, heart disease and high arches. Congestive heart failure is a common complication. There is no known treatment and prognosis is poor. Inheritance: autosomal recessive. (27 Sep 1997) |
| spinocerebellar tracts | See: anterior spinocerebellar tract, posterior spinocerebellar tract. (05 Mar 2000) |
| acute ataxia | Generalised ataxia of abrupt onset, most often caused by drug intoxications, poisonings, or vestibular neuronitis. (05 Mar 2000) |
| ataxia | <neurology> Failure of muscular coordination, irregularity of muscular action. Origin: Gr. Taxis = order (16 Dec 1997) |
| ataxia cordis | <cardiology> A condition where there is disorganised electrical conduction in the atria, resulting in ineffective pumping of blood into the ventricle. Acronym: AF (02 Jan 1998) |
| ataxia of calves | A specific cerebellar ataxia in the Jersey breed, probably a recessive genetic trait. (05 Mar 2000) |
| ataxia of lambs | Myelination failure seen in ewes on a copper-deficient diet. (05 Mar 2000) |
| ataxia-telangiectasia | <neurology, oncology> An intriguing autosomal recessive disorder in which a single defective gene produces myriad and protean effects, presents with cerebellar ataxia, telangiectasias in the eyes and skin, immune deficiency and autoimmune phenomena, propensity for lymphoid and other malignancies, excessive sensitivity to ionising radiation, increased serum alpha-fetoprotein concentrations and a tendency for chromosome breakage and translocation. A syndrome characterised by choreoathetosis beginning in childhood, progressive cerebellar ataxia, telangiectasis of conjunctiva and skin, slowly progressive mental deterioration and increasing cerebellar degeneration. There is evidence that heterozygotes show an increased susceptibility to malignancy as well, with breast cancer often cited. The gene was localised by linkage studies to chromosome 11q22-23, and recently cloned, revealing it to be homologous to the PI-3 kinase family so that prenatal diagnosis by RFLP analysis is possible. Other related genes are suspected to exist. Diagnosis in affected patients is made on clinical grounds, by detection of high concentrations of alpha-fetoprotein, and by a specialised cell culture assay for radiosensitivity and atypical radioresistant DNA synthesis. These cell culture methods are also used for prenatal diagnosis. A characteristic autopsy feature of ataxia-telangiectasia is the presence of empty basket cells in the cerebellum which results from degeneration of the previously contained Purkinje cells. Inheritance: autosomal recessive. (16 Dec 1998) |
| ataxia telangiectasia syndrome | ataxia telangiectasia |
| bovine congenital ataxia | An autosomal recessive ataxia seen in several European breeds of cattle. (05 Mar 2000) |
| Briquet's ataxia | Weakening of the muscle sense and increased sensibility of the skin, in hysteria. Synonym: hysterical ataxia. (05 Mar 2000) |
| Bruns ataxia | Difficulty in initiation of movements of the feet when they are in contact with the ground; a condition related to a frontal lobe lesion. (05 Mar 2000) |
Synonyms : Dominantly-Inherited Spinocerebellar Ataxias, Spinocerebellar Ataxia-1, Spinocerebellar Ataxia-2, Spinocerebellar Ataxia-4, Spinocerebellar Ataxia-5, Spinocerebellar Ataxia-6, Spinocerebellar Ataxia-7, Spinocerebellar Ataxias, Dominantly-Inherited
제품명 |
판매사 |
보험코드 | 성분/함량 | 구분/보험급여 |
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제품명 |
판매사 |
보험코드 | 성분/함량 | 구분/보험급여 |
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