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[Hearing loss in Townes-Brocks syndrome].

Abstract
In nineteen seventy two Towns and Brocks reported on a family in which the father and seven children showed anal atresia, triphalangeal thumb, metatarsal synostosis, extra fingers, neurosensorial deafness and ear abnormalities. The main traits were those related to hand, ear and anus alterations, transmitted under a dominant autosomal pattern. In this paper we present several members of the same family with similar alterations who finally were diagnosed of Townes-Brocks syndrome.
AuthorsJ Rodríguez Asensio, M V Rodríguez Rosell, A Ramos Pérez
JournalActa otorrinolaringologica espanola (Acta Otorrinolaringol Esp) Vol. 54 Issue 7 Pg. 518-22 ( 2003) ISSN: 0001-6519 [Print] Spain
Vernacular TitleHipoacusia en el síndrome de Townes-Brocks.
PMID14671925 (Publication Type: Case Reports, English Abstract, Journal Article)
Topics
  • Abnormalities, Multiple (genetics)
  • Adolescent
  • Adult
  • Anus, Imperforate (genetics)
  • Ear, External (abnormalities)
  • Female
  • Foot Deformities, Congenital (genetics)
  • Hand Deformities, Congenital (genetics)
  • Hearing Loss, Bilateral (diagnosis, genetics)
  • Hearing Loss, Sensorineural (diagnosis, genetics)
  • Humans
  • Male
  • Pedigree
  • Syndrome

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