Literature DB >> 2319886

An autosomal dominant inherited syndrome with congenital stapes ankylosis.

B Teunissen1, W R Cremers.   

Abstract

A newly recognized autosomal dominant inherited syndrome associated with congenital conductive deafness, hyperopia, broad thumbs, broad first toes, short distal phalanges, and syndactyly is reported. The conductive loss was the result of congenital stapes ankylosis and, in two cases, was associated with ankylosis of the short process of the incus in the fossa incudis. Stapedectomy improved hearing in these patients. Fused cervical vertebrate are also an associated feature.

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Year:  1990        PMID: 2319886     DOI: 10.1288/00005537-199004000-00009

Source DB:  PubMed          Journal:  Laryngoscope        ISSN: 0023-852X            Impact factor:   3.325


  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.  Surgery for congenital anomalies of the middle ear with mobile stapes.

Authors:  E Teunissen; C W Cremers
Journal:  Eur Arch Otorhinolaryngol       Date:  1993       Impact factor: 2.503

3.  Autosomal dominant stapes ankylosis with broad thumbs and toes, hyperopia, and skeletal anomalies is caused by heterozygous nonsense and frameshift mutations in NOG, the gene encoding noggin.

Authors:  David J Brown; Theresa B Kim; Elizabeth M Petty; Catherine A Downs; Donna M Martin; Peter J Strouse; Sayoko E Moroi; Jeff M Milunsky; Marci M Lesperance
Journal:  Am J Hum Genet       Date:  2002-06-27       Impact factor: 11.025

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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