Larsen J L, Kivlin J, Odell W D
Am J Med. 1985 Jun;78(6 Pt 1):1025-32. doi: 10.1016/0002-9343(85)90227-x.
A 24-year-old man evaluated for paresthesias and short stature was found to be hypocalcemic on initial presentation. Further evaluation showed that he had a low-normal parathormone level by amino-terminal assay, medullary stenosis of the long bones, and multiple ophthalmologic abnormalities. The remainder of his pituitary function, including growth hormone response to insulin-induced hypoglycemia, was normal. As no family history of similar findings was evident, a sporadic case of Kenny's or Kenny-Caffey syndrome was diagnosed. He became normocalcemic in response to vitamin D and calcium carbonate therapy. The results of testing in this patient and the findings in other patients previously described with the Kenny-Caffey syndrome are reviewed.
一名24岁男性因感觉异常和身材矮小接受评估,初诊时发现血钙过低。进一步评估显示,通过氨基末端检测,他的甲状旁腺激素水平略低于正常,长骨骨髓狭窄,且存在多种眼科异常。他的垂体功能其余部分,包括生长激素对胰岛素诱导的低血糖的反应,均正常。由于没有明显的类似发现家族史,诊断为散发性肯尼氏或肯尼-卡菲综合征病例。他对维生素D和碳酸钙治疗有反应,血钙恢复正常。本文回顾了该患者的检测结果以及先前描述的其他肯尼-卡菲综合征患者的发现。