Polysyndactyly-cardiac malformation syndrome

Polysyndactyly-cardiac malformation syndrome is characterized by polysyndactyly, hexadactyly (duplication of the first toe) and complex cardiac malformation (including atrial and ventricular septal defect, single ventricle, aortic dextroposition, or dilation of the right heart). It has been described in six patients from three unrelated families. Other manifestations were present in some patients (i.e. facial dysmorphism, hepatic cysts).

Also known as: Bonneau syndrome, polysyndactyly cardiac malformation, polysyndactyly with CARDIAC malformation

0 clinical trials for this condition and its sub-types, 0 tagged with Polysyndactyly-cardiac malformation syndrome itself.