Sulcus vocalis: evidence for autosomal dominant inheritance

dc.contributorUniversidade Estadual Paulista (UNESP)
dc.creatorMartins, Regina Helena Garcia
dc.creatorGoncalves, T. M.
dc.creatorNeves, D. S.
dc.creatorFracalossi, T. A.
dc.creatorTavares, E. L. M.
dc.creatorMoretti-Ferreira, D.
dc.date2014-05-20T13:36:53Z
dc.date2014-05-20T13:36:53Z
dc.date2011-01-01
dc.date.accessioned2017-04-05T20:31:56Z
dc.date.available2017-04-05T20:31:56Z
dc.identifierGenetics and Molecular Research. Ribeirao Preto: Funpec-editora, v. 10, n. 4, p. 3163-3168, 2011.
dc.identifier1676-5680
dc.identifierhttp://hdl.handle.net/11449/12693
dc.identifier10.4238/2011.December.19.5
dc.identifierWOS:000300617600089
dc.identifierWOS000300617600089.pdf
dc.identifierhttp://dx.doi.org/10.4238/2011.December.19.5
dc.identifier.urihttp://repositorioslatinoamericanos.uchile.cl/handle/2250/860259
dc.descriptionWe found evidence of autosomal dominant hereditary transmission of sulcus vocalis. Four dysphonic patients from three generations of the same family were submitted to videolaryngoscopic examination (three patients) and to direct laryngoscopy ( one patient) to diagnose the hoarseness. Sulcus vocalis was diagnosed in all four patients. The finding of four affected individuals in three generations, with vertical transmission affecting man and women, is more consistent with autosomal dominant inheritance pattern; it is an etiological model that we propose for the sulcus vocalis in this pedigree.
dc.languageeng
dc.publisherFunpec-editora
dc.relationGenetics and Molecular Research
dc.rightsinfo:eu-repo/semantics/openAccess
dc.subjectAutosomal dominant
dc.subjectSulcus vocalis
dc.subjectHoarseness
dc.subjectVideolaryngoscopy
dc.subjectGenetics
dc.subjectLaryngeal development
dc.titleSulcus vocalis: evidence for autosomal dominant inheritance
dc.typeOtro


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