| TS | 1) Tricuspid Stenosis 2) Tuberous Sclerosis = ... |
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| Bourneville | Desire-Magloire, French physician, 1840-1909. See: Bourneville's disease, Bourneville-Pringle disease. (05 Mar 2000) |
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| Bourneville's disease | <radiology> (Bourneville disease) autosomal dominant phakomatosis classic triad: seizures, retardation, adenoma sebaceum, calcified subependymal hamartomas, uncalcified tubers in cerebral cortex, enhancing lesion most likely to be malignant transformation to giant cell astrocytoma associated with: skin lesions, angiomyolipoma, increased risk of renal cell carcinoma (12 Dec 1998) |
| Bourneville-Pringle disease | Facial lesions with tuberous sclerosis, first reported as adenoma sebaceum, but now recognised as angiofibromas. (05 Mar 2000) |
| Bourneville-Pringle syndrome |
(Bourne
Ãâó: www.mercksource.com/pp/us/cns/cns_hl_dorlands.jspz...
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| Bourneville's disease |
(Bourne
Ãâó: www.mercksource.com/pp/us/cns/cns_hl_dorlands.jspz...
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| Bourneville's disease |
Tuberous sclerosis, (meaning "hard potatoes") is a rare genetic, disorder primarily characterized by a triad of seizures, mental retardation, and skin lesions (called adenoma sebaceum). This "classic" Vogt triad is present in 30-50% of cases; in particular, up to 30% of tuberous sclerosis reportedly have normal mentation. ...
Ãâó: en.wikipedia.org/wiki/Bourneville's_disease
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| Bourneville-Pringle disease |
Tuberous sclerosis, (meaning "hard potatoes") is a rare genetic, disorder primarily characterized by a triad of seizures, mental retardation, and skin lesions (called adenoma sebaceum). This "classic" Vogt triad is present in 30-50% of cases; in particular, up to 30% of tuberous sclerosis reportedly have normal mentation. ...
Ãâó: en.wikipedia.org/wiki/Bourneville-Pringle_disease
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| Bourneville's d. |
tuberous sclerosis.
Ãâó: www.mercksource.com/pp/us/cns/cns_health_library.j...
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