Richiericosta, A.Guionalmeida, M. L.Lauris, JRPFerreira, D. M.2014-05-202014-05-201994-01-15American Journal of Medical Genetics. New York: Wiley-liss, v. 49, n. 2, p. 224-228, 1994.0148-7299http://hdl.handle.net/11449/38928We report on 2 brothers, born to consanguineous parents presenting thin/long face, small ears, blepharophimosis, malar hypoplasia, long neck, pectus excavatum, brachy-camptodactyly, and sacral dimple. We suspect that these patients represent a previously undescribed autosomal recessive syndrome. (C) 1994 Wiley-Liss, Inc.224-228engBLEPHAROPHIMOSISSMALL EARSCAMPTODACTYLYPECTUS EXCAVATUMCONSANGUINITYAUTOSOMAL RECESSIVE INHERITANCEArtigo10.1002/ajmg.1320490213WOS:A1994MP33000012Acesso restrito6250622352641608