Texto completo: acesso restrito. p. 570–571 Submitted by Edileide Reis (leyde-landy@hotmail.com) on 2014-05-15T14:23:19Z No. of bitstreams: 1 Victor Diniz de Pochat.pdf: 13787248 bytes, checksum: df458f0b017d37aef6f66c126a0a7a3d (MD5) Approved for entry into archive by Patricia Barroso (pbarroso@ufba.br) on 2014-08-11T19:06:18Z (GMT) No. of bitstreams: 1 Victor Diniz de Pochat.pdf: 13787248 bytes, checksum: df458f0b017d37aef6f66c126a0a7a3d (MD5) Made available in DSpace on 2014-08-11T19:06:18Z (GMT). No. of bitstreams: 1 Victor Diniz de Pochat.pdf: 13787248 bytes, checksum: df458f0b017d37aef6f66c126a0a7a3d (MD5) Previous issue date: 2012 Abstract: Ascher syndrome is defined by the association between double lip, blepharochalasis, and nontoxic goiter. Because it is a rare disease, it is most often misdiagnosed, despite its implications for quality of life. We report a variation of an incomplete type of Ascher syndrome affecting the upper lip, upper eyelids, and lateral canthi of a young male patient. The surgical management, follow-up, and a brief overview of the syndrome are described. The results presented show an aesthetic and functional improvement of the facial deformities.