| 释义 |
Sturge–Weber Path.|stɜːdʒ ˈwɛbə(r)|
[The names of W. A. Sturge (1850–1919) and F. P. Weber (1863–1962), English physicians, who described the syndrome in 1879 and 1922 respectively.]
Sturge–Weber syndrome or Sturge–Weber 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.
1935H. 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. 1974J. H. Menkes Textbk. Child Neurol. x. 412/2 The coincidence of a facial vascular disease and seizures suggests Sturge–Weber disease. |