Pandey Dharmendra B, Pednekar Sangeeta J, Chavan Swati A, Korivi Deepa, Shah Amit Kumar, Kulkarni Uday P
Department of Medicine, Lokmanya Tilak Municipal Medical College and General Hospital, Sion, Mumbai - 400 022.
J Assoc Physicians India. 2011 Jul;59:447-9.
Here we report a case of VACTERL ASSOCIATION in a twenty three years old married female patient primigravida with 3 months of amenorrhea admitted with history of fever and gastroenteritis along with congenital developmental defects such as scoliosis (V), small ventricular septal defect (C), right sided hemifacial dysmorphic features (right mandibular hypoplasia), small sized right sided kidney (R), bilateral hypoplastic thumb (L). For the diagnosis of VACTERL atleast three out of seven anomalies should be present while our patient had four anomalies.
在此，我们报告一例23岁已婚初孕女性患者的VACTERL综合征，该患者停经3个月，因发热、肠胃炎病史入院，同时伴有先天性发育缺陷，如脊柱侧弯（V）、小型室间隔缺损（C）、右侧面部畸形特征（右侧下颌发育不全）、右侧小肾（R）、双侧拇指发育不全（L）。对于VACTERL综合征的诊断，至少应出现七项异常中的三项，而我们的患者有四项异常。
