| Literature DB >> 22687844 |
Zheng Shen1, Chao Chun Zou, Shi Qiang Shang, Ke Wen Jiang.
Abstract
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.Entities:
Mesh:
Year: 2012 PMID: 22687844 DOI: 10.2169/internalmedicine.51.7097
Source DB: PubMed Journal: Intern Med ISSN: 0918-2918 Impact factor: 1.271