Maddox J L, Odom R B, Goette D K
Pediatr Dermatol. 1984 Apr;1(4):307-11. doi: 10.1111/j.1525-1470.1984.tb01135.x.
Menkes's syndrome (trichopoliodystrophy) is an x-linked, recessive genodermatosis characterized by hair defects, severe retardation, convulsions, progressive neurologic deterioration, and early death. Recent studies in copper metabolism suggest that Menkes's syndrome may be a storage disease in which copper is irreversibly trapped in some tissues by metallothionein, a heavy-metal-binding protein. This then gives rise to a deficiency elsewhere, particularly in the brain, causing irreversible damage in the fetus. We present a patient with Menkes's syndrome and review the clinical and metabolic aspects of this disease.
门克斯综合征(毛发硫营养不良)是一种X连锁隐性遗传性皮肤病,其特征为毛发缺陷、严重发育迟缓、惊厥、进行性神经功能恶化及早期死亡。最近关于铜代谢的研究表明,门克斯综合征可能是一种贮积病,其中铜被重金属结合蛋白金属硫蛋白不可逆地滞留在某些组织中。这进而导致其他部位,尤其是大脑出现铜缺乏,对胎儿造成不可逆损害。我们报告1例门克斯综合征患者,并对该疾病的临床和代谢方面进行综述。