Copper metabolism study in oculocutaneous albinism.

B Silverstone, D Mendelsohn
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Abstract

Abnormal copper metabolism has been described in some pigmentary retinopathies. Albinism is a manifestation of a metabolic disorder in which lack of pigmentation is a prominent feature and changes in the retinal pigment epithelium are found as well. We examined the blood and urine of two groups of patients, albino and control groups, for copper, zinc and ceruloplasmin in serum and copper excretion in urine. We found in the albino group, elevated values of ceruloplasmin which was highly significant when compared to the control group. The mean copper concentration in serum was found to be high as well. The urinary copper was distinctly elevated in four patients of the albino group. Therefore, our results suggest that there might be a primary abnormality of copper metabolism in these patients.

皮肤白化病患者铜代谢的研究。
铜代谢异常已被描述为一些色素视网膜病变。白化病是一种代谢紊乱的表现,其中缺乏色素沉着是一个突出的特征,视网膜色素上皮的变化也被发现。我们检测了白化病和对照组两组患者的血、尿中铜、锌、铜蓝蛋白的含量和尿中铜的排泄量。我们发现,与对照组相比,白化病组铜蓝蛋白升高非常显著。血清中铜的平均浓度也较高。白化病组4例患者尿铜明显升高。因此,我们的结果表明,这些患者可能存在铜代谢的原发性异常。
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