[克-特综合征，一例报告]

Padiatr Grenzgeb. 1989;28(3):185-8.

Description of the Klippel-Trénaunay-Syndrome; it could have been sporadic found in a 3; 6-year-old girl. This congenital anomaly is characterized by haemangiomatosis, varicosis and unilateral hypertrophia of limbs. As a rule the therapy is a symptomatic one, surgical operations concerning the skeleton are infrequent.

克-特-魏综合征的描述；该病症可能散发于一名3至6岁女童。这种先天性异常的特征为血管瘤病、静脉曲张和单侧肢体肥大。通常治疗是对症治疗，涉及骨骼的外科手术并不常见。