Kristoferitsch W, Pointner H
J Neurol. 1987 Feb;234(2):116-8. doi: 10.1007/BF00314115.
A case of slowly progressing cerebellar syndrome and pathologically confirmed adult coeliac disease is presented. Neurological symptoms progressed although the patient had no enteric complaints. This case seems to be identical with 18 previously reported cases of encephalopathy and adult coeliac disease. However, the aetiology and pathogenesis of the encephalopathy are still not known.
本文报告一例进展缓慢的小脑综合征且经病理证实为成人乳糜泻的病例。尽管患者没有肠道不适症状,但神经症状仍在进展。该病例似乎与先前报道的18例脑病合并成人乳糜泻病例相同。然而,脑病的病因和发病机制仍不清楚。