Gautier E, Frenk E, Uske A, Queloz J, Laurini R
Service de Pédiatrie, CHUV, Lausanne.
Helv Paediatr Acta. 1989 Feb;43(4):333-44.
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.
作者描述了一名自出生起就患有严重结缔组织病的患者,伴有病理性骨折、耳廓软骨缺失、手指过度松弛以及皮肤松弛且有深褶皱,所有这些都提示胶原蛋白和弹性蛋白紊乱。出生24小时时的体温过低就已提示可能患有门克斯综合征。从第3个月起,患者出现神经功能恶化和难治性肌阵挛癫痫。颅脑计算机断层扫描显示,随着时间推移,出现脑萎缩和硬膜下血肿。心脏超声心动图检查发现冠状动脉血管发育异常。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。皮肤活检的电子显微镜检查显示表皮桥粒异常。桥粒分离,提示桥粒间黏合物质发生改变。