Literature DB >> 10337976

Proximal symphalangism and congenital conductive hearing loss: otologic aspects.

R J Ensink1, J P Sleeckx, C W Cremers.   

Abstract

OBJECTIVE: Results of stapedectomy are reported in a Belgian 26-year-old woman and two Dutch brothers having the proximal symphalangism syndrome (McKusick 18580). STUDY
DESIGN: Case reports are presented. A review of the results of ear surgery for congenital conductive hearing loss in this syndrome is given.
SETTING: The Belgian patient was treated in a general hospital. The Dutch patients were treated in a university hospital, which was a tertiary referral center. PATIENTS: Patients were referred to have an evaluation of their hearing impairment. INTERVENTION: Based on the syndromal diagnosis and based on routine audiometric tests, a congenital ossicular fixation was considered to be the cause of the hearing loss. By exploratory tympanotomies, this was confirmed. Reconstructive procedures including stapedotomy were performed. MAIN OUTCOME MEASURES/
RESULTS: Long-term audiometric data are presented to evaluate the outcome of the surgical interventions.
CONCLUSIONS: Congenital stapes ankylosis eventually combined with a congenital fixation of the short process of the incus in the fossa incudis, causing the congenital conductive hearing loss. Surgical intervention is very successful in most reported cases, but negative side effects are incidentally found as well.

Entities:  

Mesh:

Year:  1999        PMID: 10337976

Source DB:  PubMed          Journal:  Am J Otol        ISSN: 0192-9763


  7 in total

1.  Identification of two novel mutations in the NOG gene associated with congenital stapes ankylosis and symphalangism.

Authors:  Akira Ganaha; Tadashi Kaname; Yukinori Akazawa; Teruyuki Higa; Ayano Shinjou; Kenji Naritomi; Mikio Suzuki
Journal:  J Hum Genet       Date:  2014-11-13       Impact factor: 3.172

2.  Role of hindbrain in inner ear morphogenesis: analysis of Noggin knockout mice.

Authors:  Jinwoong Bok; Lisa J Brunet; Omar Howard; Quianna Burton; Doris K Wu
Journal:  Dev Biol       Date:  2007-08-16       Impact factor: 3.582

3.  Temporal Bone Histopathology in NOG-Symphalangism Spectrum Disorder.

Authors:  Alicia M Quesnel; Joseph B Nadol; G Petur Nielsen; Hugh D Curtin; Marci M Lesperance
Journal:  Otol Neurotol       Date:  2015-12       Impact factor: 2.311

4.  Mutations in the NOG gene are commonly found in congenital stapes ankylosis with symphalangism, but not in otosclerosis.

Authors:  S Usami; S Abe; S Nishio; Y Sakurai; H Kojima; T Tono; N Suzuki
Journal:  Clin Genet       Date:  2012-01-30       Impact factor: 4.438

5.  Genetic and clinical phenotypic analysis of familial stapes sclerosis caused by an NOG mutation.

Authors:  Rong Yu; Hongqun Jiang; Huihuang Liao; Wugen Luo
Journal:  BMC Med Genomics       Date:  2020-12-11       Impact factor: 3.063

6.  Genetic Heterogeneity and Core Clinical Features of NOG-Related-Symphalangism Spectrum Disorder.

Authors:  Ryan J Carlson; Alicia Quesnel; Dawson Wells; Zippora Brownstein; Dror Gilony; Suleyman Gulsuner; Kathleen A Leppig; Karen B Avraham; Mary-Claire King; Tom Walsh; Jay Rubinstein
Journal:  Otol Neurotol       Date:  2021-09-01       Impact factor: 2.619

7.  A novel nonsense mutation in the NOG gene causes familial NOG-related symphalangism spectrum disorder.

Authors:  Kenichi Takano; Noriko Ogasawara; Tatsuo Matsunaga; Hideki Mutai; Akihiro Sakurai; Aki Ishikawa; Tetsuo Himi
Journal:  Hum Genome Var       Date:  2016-08-04
  7 in total

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