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单词 sturge–weber syndrome or disease
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Sturge–Weber syndrome or disease
Sturge–Weber syndrome or disease: a congenital syndrome in which a diffuse malformation of blood vessels on one side of the head produces port-wine nævus on the face and lesions of the brain, usually resulting in fits and mental retardation.
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the world > health and disease > ill health > a disease > congenital or hereditary syndromes > [noun]
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congenital myotonia1886
myotonia congenita1887
Thomsen's disease1890
von Recklinghausen's disease1899
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myotonia atrophica1908
Fröhlich1909
Milroy's disease1909
Lindau disease1928
Steinert's disease1932
von Hippel–Lindau disease1932
Werner's syndrome1934
Sturge–Weber syndrome1935
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Morgagni's syndrome1936
Hurler's disease1937
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Turner1942
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Klinefelter1950
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the world > health and disease > ill health > a disease > disorders of internal organs > disorders of nervous system > [noun] > disorders of brain > other brain disorders
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1935 H. Bergstrand in Abstr. 2nd Internat. Neurol. Congr., London 124 Sturge–Weber's disease is a syndrome comparable with von Recklinghausen's..and Bourneville's diseases.
1974 J. H. Menkes Textbk. Child Neurol. x. 412/2 The coincidence of a facial vascular disease and seizures suggests Sturge–Weber disease.
extracted from Sturge–Webern.
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