Suppr超能文献

金-登博罗综合征:挛缩测试与文献综述

King-Denborough syndrome: contracture testing and literature review.

作者信息

Heiman-Patterson T D, Rosenberg H R, Binning C P, Tahmoush A J

机构信息

Department of Neurology, Hahnemann University Hospital, Philadelphia, PA 19102.

出版信息

Pediatr Neurol. 1986 May-Jun;2(3):175-7. doi: 10.1016/0887-8994(86)90013-5.

Abstract

The King-Denborough syndrome (KDS) is characterized by dysmorphic features, myopathy, and malignant hyperthermia (MH). Physiologic contracture testing for MH susceptibility has not been reported in KDS. A young boy with KDS underwent muscle biopsy evaluation at age 3 years that documented an abnormal contracture response to halothane, indicating MH susceptibility. Histopathology demonstrated small type II fibers associated with type I hypertrophy. Contracture testing of muscle obtained from the patient's mother was positive, while a sibling's test was negative. This case is the first to demonstrate susceptibility to MH with KDS by using physiologic contracture testing. The presence of positive MH results in both the patient and his mother suggest one of the following: (1) KDS may be part of the spectrum of autosomal dominantly inherited MH; (2) the locus for MH and for KDS may be linked closely and inherited concurrently, or; (3) the association of MH and KDS may be coincidental.

摘要

金-丹伯勒综合征(KDS)的特征为畸形体征、肌病和恶性高热(MH)。尚未有关于KDS患者进行MH易感性生理挛缩试验的报道。一名患有KDS的小男孩在3岁时接受了肌肉活检评估,结果显示其对氟烷的挛缩反应异常,表明存在MH易感性。组织病理学显示存在小型II型纤维并伴有I型纤维肥大。对患者母亲的肌肉进行挛缩试验结果为阳性,而其一名兄弟姐妹的试验结果为阴性。该病例是首例通过生理挛缩试验证实KDS患者存在MH易感性的病例。患者及其母亲的MH结果均为阳性提示以下情况之一:(1)KDS可能是常染色体显性遗传MH谱系的一部分;(2)MH和KDS的基因座可能紧密连锁并同时遗传,或者;(3)MH与KDS之间的关联可能是巧合。

文献检索

告别复杂PubMed语法,用中文像聊天一样搜索,搜遍4000万医学文献。AI智能推荐,让科研检索更轻松。

立即免费搜索

文件翻译

保留排版,准确专业,支持PDF/Word/PPT等文件格式,支持 12+语言互译。

免费翻译文档

深度研究

AI帮你快速写综述,25分钟生成高质量综述,智能提取关键信息,辅助科研写作。

立即免费体验