Shen Zheng, Zou Chao Chun, Shang Shi Qiang, Jiang Ke Wen
Department of Pediatrics, the Children's Hospital of Zhejiang University School of Medicine and Zhejiang Key Laboratory for Diagnosis and Therapy of Neonatal Diseases, China.
Intern Med. 2012;51(11):1371-4. doi: 10.2169/internalmedicine.51.7097. Epub 2012 Jun 1.
Congenital heart disease (CHD) is extremely rarely reported in 48, XYY, +21 karyotype. Herein, we reported one case of 48,XYY,+21 karyotype with CHD and reviewed the available literature. The phenotypic characteristics of the 4-month-old child showed the presence of features typical of mongoloid slant. X-ray detection showed the form of heart was corpulent and the bilateral mediastinum was broad. Doppler echocardiogram detection showed atrial septal and ventricular septal defects with patent ductus arteriosus, pulmonary hypertension and mild tricuspid regurgitation. Including this case, 63 cases of 48, XYY, +21 chromosome pattern have been reported. However, only 9 cases have CHD.
先天性心脏病(CHD)在48,XYY,+21核型中极为罕见。在此,我们报告1例48,XYY,+21核型合并CHD的病例,并回顾现有文献。该4个月大儿童的表型特征显示有典型的蒙古样斜眼特征。X线检查显示心脏外形饱满,双侧纵隔增宽。多普勒超声心动图检查显示房间隔和室间隔缺损、动脉导管未闭、肺动脉高压和轻度三尖瓣反流。包括本病例在内,已报告63例48,XYY,+21染色体模式。然而,仅有9例合并CHD。