Whistling face syndrome. A case report and literature review.

Acta paediatrica Hungarica Pub Date : 1991-01-01
M M Millner, I D Mutz, W Rosenkranz
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引用次数: 0

Abstract

The cranio-carpo-tarsal or "whistling face" syndrome was first described by Freeman and Sheldon in 1938. More than 60 cases with great variability of expression are known till now and autosomal dominant as well as recessive inheritance and sporadic cases suggest a genetic heterogeneity. We review 60 well-documented cases of the literature and present a patient with a severe form, who died of bronchopneumonia at the age of 9 months. The facial stigmata of his mother and the ulnar deviations of his maternal grandfather support the autosomal inheritance of the syndrome.

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吹口哨脸综合症。病例报告及文献复习。
1938年,弗里曼和谢尔登首次描述了颅-腕骨-跗骨综合征。目前已知有60多例表达差异较大的病例,常染色体显性遗传、隐性遗传和散发病例提示存在遗传异质性。我们回顾了60个有充分记录的文献病例,并提出了一个严重形式的患者,在9个月大时死于支气管肺炎。他母亲的面部斑点和他外祖父的尺骨偏差支持常染色体遗传综合征。
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