Najim al-Din A S, Wriekat A, Mubaidin A, Dasouki M, Hiari M
Jordan University Hospital, Amman.
Acta Neurol Scand. 1994 May;89(5):347-52. doi: 10.1111/j.1600-0404.1994.tb02645.x.
An unusual neurological syndrome in an Arab family with five affected siblings, is reported. Autosomal recessive inheritance is suggested by having multiple affected siblings born to phenotypically normal consanguineous parents. Similar to Davison's Pallido-pyramidal syndrome, they presented with the clinical signs and symptoms of severe parkinsonism as well as evidence of cortico-spinal tract disease. In addition, they had dementia and supranuclear upgaze paresis. MRI studies showed significant atrophy of the globus pallidus and the pyramids, as well as generalized brain atrophy in later stages. Therapy with levodopa resulted in significant improvement in the extrapyramidal dysfunction. We suggest that this probably represents a new syndrome which is closely related but not identical to the pallido-pyramidal syndrome.
报告了一个阿拉伯家庭中五名患病兄弟姐妹的一种罕见神经综合征。多个患病兄弟姐妹由表型正常的近亲父母所生,提示为常染色体隐性遗传。与戴维森苍白球 - 锥体综合征相似,他们表现出严重帕金森病的临床体征和症状以及皮质脊髓束疾病的证据。此外,他们还有痴呆和核上性上视麻痹。磁共振成像(MRI)研究显示苍白球和锥体有明显萎缩,后期还有全脑萎缩。左旋多巴治疗使锥体外系功能障碍有显著改善。我们认为这可能代表一种新综合征,与苍白球 - 锥体综合征密切相关但并不相同。