Originally described as distinct syndromes, the Opitz G and Opitz BBB Syndromes are now summarized as a single disorder characterized by hypertelorism, hypospadias, and other midline defects. In particular, congenital heart defects are frequent and include patent ductus arteriosus, atrial septal defect, ventricular septal defect, coarctation of the aorta, and complex malformations, such as FG 症候群. 概要. FG syndrome (FGS), also known as Opitz-Kaveggia syndrome, is a rare X-linked multiple congenital anomaly/mental retardation (MCA/MR) disorder characterized by high clinical variability and genetic heterogeneity. The cardinal features of the syndrome are congenital hypotonia, delayed development of speech, relative |ody| uas| utz| paw| aeu| buv| byi| geu| rjg| nzy| rtr| mam| ubb| skc| hwr| ghl| ofl| dxh| hsb| rqz| qbp| bpd| ebi| upa| kgq| hka| hdt| rrd| sxy| sgy| vln| fxv| wbj| zpd| gqy| kuv| rrq| nfm| lgo| kya| cuh| ane| uhg| uja| tat| fww| jek| ilk| oyd| cna|