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魁北克眼咽型肌营养不良症中的核内包涵体。

Nuclear inclusions in oculopharyngeal muscular dystrophy in Quebec.

作者信息

Bouchard J P, Gagné F, Tomé F M, Brunet D

机构信息

Hôpital de l'Enfant-Jésus, Université Laval, Québec, P.Q., Canada.

出版信息

Can J Neurol Sci. 1989 Nov;16(4):446-50. doi: 10.1017/s0317167100029565.

Abstract

Seven French-Canadian cases of clearcut oculopharyngeal muscular dystrophy (OPMD) had their muscle studied for the presence of intranuclear inclusions, and they were all positive. Inclusions of both "mature" and "immature" types were seen in our material. The presence of such intranuclear structures should be added to the criteria of the clinical picture and the family history for diagnosis of a case and inclusion of a family in further genetic studies. Reverse genetic studies of large families and biochemical studies of these intranuclear structures may help to understand the pathogenesis of this common disease in Quebec.

摘要

对七例明确诊断为眼咽型肌营养不良症(OPMD)的法裔加拿大人病例的肌肉进行了研究,以检测核内包涵体的存在,结果均呈阳性。在我们的材料中观察到了“成熟”和“不成熟”两种类型的包涵体。在诊断病例和将家族纳入进一步的基因研究时,应将这种核内结构的存在纳入临床表现和家族史的诊断标准中。对大家庭进行反向基因研究以及对这些核内结构进行生化研究,可能有助于了解魁北克这种常见疾病的发病机制。

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