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缺乏merosin和merosin阳性的先天性肌营养不良的临床和组织病理学研究。

Clinical and histopathological study of merosin-deficient and merosin-positive congenital muscular dystrophy.

作者信息

Talim B, Kale G, Topaloglu H, Akçören Z, Caglar M, Gögüş S, Elkay M

机构信息

Department of Pediatric Pathology, Hacettepe Children's Hospital, 06100 Ankara, Turkey.

出版信息

Pediatr Dev Pathol. 2000 Mar-Apr;3(2):168-76. doi: 10.1007/s100240050021.

Abstract

The clinical features of merosin-positive congenital muscular dystrophy (CMD) and merosin-deficient CMD are well known, with those of merosin-deficient CMD being more severe. Whether the severity of histopathological findings correlates with these clinical features remains unanswered. In this study, the clinical and histopathological findings of 39 merosin-deficient and 37 merosin-positive CMD patients were compared. Merosin-deficient CMD patients were found to be younger, with earlier onset of symptoms, age of diagnosis, and a more severe clinical state (reflecting maximum motor capacity and contractures). On histopathological evaluation, endomysial fibrosis, perimysial fibrosis, and histopathological state (reflecting fibrosis, adiposis, necrosis, and variation in fiber size) were more severe in merosin-deficient CMD. There was a correlation between clinical and histopathological states only in merosin-deficient CMD.

摘要

肌膜素阳性先天性肌营养不良(CMD)和肌膜素缺乏型CMD的临床特征已为人熟知,其中肌膜素缺乏型CMD的症状更为严重。组织病理学检查结果的严重程度是否与这些临床特征相关仍未得到解答。在本研究中,对39例肌膜素缺乏型CMD患者和37例肌膜素阳性CMD患者的临床和组织病理学检查结果进行了比较。结果发现,肌膜素缺乏型CMD患者年龄更小,症状出现更早,确诊年龄更小,临床状态更严重(反映最大运动能力和挛缩情况)。在组织病理学评估中,肌膜素缺乏型CMD的肌内膜纤维化、肌束膜纤维化和组织病理学状态(反映纤维化、脂肪变性、坏死和纤维大小变化)更为严重。仅在肌膜素缺乏型CMD中,临床状态与组织病理学状态之间存在相关性。

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