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Case Reports
Facio-genito-popliteal syndrome presenting with bilateral choanal atresia and maxillary hypoplasia.
- E Vandeweyer, F C Urbain, and A DeMey.
- Plastic and Reconstructive Surgery Department, University Hospital Brugmann, Brussels, Belgium.
- Br J Plast Surg. 2000 Jan 1; 53 (1): 65-7.
AbstractThe 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.Copyright 2000 The British Association of Plastic Surgeons.
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