Bijulal, SasidharanSivasankaran, SivasubramanianKrishnamoorthy, Kavassery MTitus, ThomasTharakan, Jaganmohan AKrishnamanohar, Soman R2012-12-042012-12-042008Congenital heart disease. 3; 3; 205-8http://dx.doi.org/10.1111/j.1747-0803.2008.00193.xhttps://dspace.sctimst.ac.in/handle/123456789/1257OBJECTIVES: To report the clinical features, nature of vasculopathy observed and the management instituted in three cases of PHACE syndrome.RESULTS: All three patients were noted to have diffuse vasculopathy and aortic arch hypoplasia in addition to aortic coarctation adding substantial surgical risk or making surgery palliative.CONCLUSION: PHACE syndrome should be considered in the differential diagnosis of aortic coarctation associated with aortic arch hypoplasia.CardiologyUnusual coarctation-the PHACE syndrome: report of three cases.