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Facio-genito-popliteal syndrome presenting with bilateral choanal atresia and maxillary hypoplasia
E Vandeweyer1, F C Urbain, A DeMey
1Plastic and Reconstructive Surgery Department, University Hospital Brugmann, Brussels, Belgium.
British Journal of Plastic Surgery
|February 5, 2000
Abstract:
The most classic characteristics of facio-genito-popliteal syndrome are cleft lip and/or palate, anomalies of the external genitalia and popliteal pterygium. A case of facio-genito-popliteal syndrome with bilateral choanal atresia and maxillary hypoplasia is presented. No previous report of such an association was found in the literature.