Literature DB >> 10743764

Spondyloepiphyseal dysplasia congenita associated with conductive hearing loss.

R Dahiya1, S Cleveland, C A Megerian.   

Abstract

Spondyloepiphyseal dysplasia is a disorder characterized by abnormalities of growth. Previous studies of this disorder have identified a significant incidence of associated hearing loss. Hearing loss has been reported to occur in 25 to 30% of affected patients. To date, all reports of associated hearing loss have indicated the presence of a sensorineural component. In this article, we report the case of a child who was diagnosed with spondyloepiphyseal dysplasia congenita and who was found to have a significant conductive hearing loss with a Carhart's notch, indicating the likely presence of stapes footplate fixation. We also review the diagnosis of this condition and the literature associated with hearing loss as it occurs with this disorder.

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Year:  2000        PMID: 10743764

Source DB:  PubMed          Journal:  Ear Nose Throat J        ISSN: 0145-5613            Impact factor:   1.697


  4 in total

Review 1.  Molecular genetics and metabolism, special edition: Diagnosis, diagnosis and prognosis of Mucopolysaccharidosis IVA.

Authors:  Hira Peracha; Kazuki Sawamoto; Lauren Averill; Heidi Kecskemethy; Mary Theroux; Mihir Thacker; Kyoko Nagao; Christian Pizarro; William Mackenzie; Hironori Kobayashi; Seiji Yamaguchi; Yasuyuki Suzuki; Kenji Orii; Tadao Orii; Toshiyuki Fukao; Shunji Tomatsu
Journal:  Mol Genet Metab       Date:  2018-05-15       Impact factor: 4.797

2.  A novel mutation in COL2A1 leading to spondyloepiphyseal dysplasia congenita in a three-generation family.

Authors:  Leilei Xu; Xusheng Qiu; Zezhang Zhu; Long Yi; Yong Qiu
Journal:  Eur Spine J       Date:  2014-04-16       Impact factor: 3.134

3.  Identification of a novel mutation of the COL2A1 gene in a Chinese family with spondyloepiphyseal dysplasia congenita.

Authors:  Hongzhuo Li; Liang Ma; Baozhu Wang; Yun Cui; Tao Xiao
Journal:  Eur Spine J       Date:  2015-05-13       Impact factor: 3.134

4.  Discovery of sensorineural hearing loss and ossicle deformity in a Chinese Li nationality family with spondyloepiphyseal dysplasia congenita caused by p.G504S mutation of COL2A1.

Authors:  Kan Wu; Zhumei Li; Yuhua Zhu; Xiaocheng Wang; Guohui Chen; Zhaohui Hou; Qiujing Zhang
Journal:  BMC Med Genomics       Date:  2021-06-28       Impact factor: 3.063

  4 in total

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