(门克斯疾病。结缔组织明显受累及表皮桥粒改变1例报告。

Helvetica paediatrica acta Pub Date : 1989-02-01
E Gautier, E Frenk, A Uske, J Queloz, R Laurini
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引用次数: 0

摘要

作者描述了一个患者从出生开始就表现为结缔组织严重受累,伴有病理性骨折,缺乏耳软骨,手指过度松弛,皮肤松弛伴深褶皱,所有提示胶原蛋白和弹性蛋白紊乱。24小时时体温过低应该已经预示着门克斯综合征的可能性。从第3个月起,患者出现神经系统恶化和肌阵挛性癫痫,治疗无效。颅脑断层密度测量显示,随着时间的推移,脑萎缩和硬脑膜下血肿。超声心动图显示冠状动脉血管发育不全。血清铜和铜蓝蛋白水平检测不到,体外成纤维细胞对铜的摄取增加,证实了门克斯综合征的诊断。皮肤活组织检查的电子显微镜显示表皮的桥粒体异常。桥粒保持分开表明桥粒间黏结发生了改变。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
[Menkes disease. Report of a case with pronounced involvement of connective tissues and changes in epidermal desmosomes].

The authors describe a patient who presented from birth on a severe involvement of connective tissues with pathological fractures, lack of auricular cartilage, hyperlaxity of fingers and cutis laxa with deep folds, all suggestive of derangements of collagen and elastin. Hypothermia at 24 hours of age should have already indicated the possibility of Menkes' syndrome. From the 3rd month on, the patient presents a neurological deterioration and a myoclonic epilepsy which is resistant to treatment. Craniocerebral tomodensitometry revealed, with time, a cerebral atrophy and subdural hematomas. Angiodysplasia of a coronary artery was seen at cardiac echocardiography. Undetectable levels of serum copper and ceruloplasmin, and an increased uptake of copper by fibroblasts in vitro confirmed the diagnosis of Menkes' syndrome. Electron microscopy of a skin biopsy disclosed a desmosomal anomaly in the epidermis. Desmosomes stay apart suggesting an alteration of the interdesmosomal cement.

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