| Krabbe's disease | <radiology> Dysmyelinating disease, autosomal recessive, usually presents by 1 yr, specific enzyme deficiency identified, rapid spontaneous nystagmus, poikilothermia Synonym: Krabbe leukodystrophy (12 Dec 1998) |
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| Christensen-Krabbe disease | Familial progressive spastic paresis of extremities with progressive mental deterioration, with development of seizures, blindness and deafness, beginning during the first year of life, and with destruction and disorganization of nerve cells of the cerebral cortex. Synonym: Alpers disease, Christensen-Krabbe disease, progressive cerebral poliodystrophy. (05 Mar 2000) |
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| Krabbe, Knud | <person> Danish neurologist, 1885-1961. See: Krabbe's disease, Christensen-Krabbe disease. (05 Mar 2000) |
| Krabbe's d. |
a lysosomal storage disease due to a deficiency of galactosylceramidase. It begins in infancy with irritability, fretfulness, and rigidity, followed by tonic seizures, convulsions, quadriplegia, blindness, deafness, dysphagia, and progressive mental deterioration. Pathologically, there is rapidly progressive cerebral demyelination and large globoid bodies in the white substance. Called also galactosylceramide lipidosis and globoid cell or Krabbe's leukodystrophy.
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| Krabbe's disease (leukodystrophy) |
see under disease.
Ãâó: www.mercksource.com/pp/us/cns/cns_health_library.j...
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| Krabbe's l. |
see under disease.
Ãâó: www.mercksource.com/pp/us/cns/cns_health_library.j...
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