Churesigaew S
Division of Endocrinology, Children's Hospital, Bangkok, Thailand.
J Med Assoc Thai. 1994 Oct;77(10):554-9.
Kenny-Caffe Syndrome is rarely found. From 1966-1993 only 22 cases were reported worldwide. The author presented a case of Kenny-Caffe Syndrome who showed typical findings, i.e. short stature, small slender long bones with medullary stenosis, thickened cortex of the long bones, hypocalcemia with tetany at 1 month of age, hyperphosphatemia, hyperopia of both eyes and normal IQ. A review of the literature summarizing the clinical and laboratory findings of this syndrome is also presented.
肯尼 - 卡菲综合征极为罕见。1966年至1993年期间,全球仅报告了22例。作者报告了一例肯尼 - 卡菲综合征患者,该患者表现出典型症状,即身材矮小、细长的长骨伴有骨髓狭窄、长骨皮质增厚、1个月大时出现低钙血症并伴有手足搐搦、高磷血症、双眼远视且智商正常。本文还对该综合征的临床和实验室检查结果进行了文献综述。