FATCO syndrome: a new case and review of the literature

Fibular aplasia, tibial campomelia, and oligosyndactyly (fatco) syndrome is a very rare syndrome. the inheritance pattern of this syndrome and responsible gene or genes are unclear. until today, only 14 patients have been reported. herein, we have presented a new male patient with fatco syndrome. in order to define the clinical features other than the major ones, we had an overview of the phenotypical findings of this rare syndrome by comparing the clinical findings of our case with those of the published cases