Literature DB >> 8694130

Hearing impairment in Engelmann disease.

K Higashi1, C Matsuki.   

Abstract

There are several hyperostosis diseases of the skull that are accompanied by hearing impairment. In this article a case of Engelmann disease is presented. Currently > 130 cases of Engelmann disease are reported in literature. About 18% of these cases reported hearing impairment, but it is possible that this figure may be higher, because many of the authors concentrated on other aspects of the disease and made no reference to hearing loss in their reports. The etiology of deafness is the narrowing of the internal auditory canals cause by bony encroachment on nerves and vessels. This lends to progressive perceptive hearing loss and narrowing of the tympanic cavities. The result is fixation or adhesion of ossicle to tympanic walls, and narrowing of the bony part of auditory tubes, which causes serous otitis media.

Entities:  

Mesh:

Year:  1996        PMID: 8694130

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


  6 in total

1.  Camurati-Engelmann's disease: a case report.

Authors:  Rosemary Kusaba Byanyima; Jennifer Batuuka Nabawesi
Journal:  Afr Health Sci       Date:  2002-12       Impact factor: 0.927

2.  Tissue-specific calibration of extracellular matrix material properties by transforming growth factor-β and Runx2 in bone is required for hearing.

Authors:  Jolie L Chang; Delia S Brauer; Jacob Johnson; Carol G Chen; Omar Akil; Guive Balooch; Mary Beth Humphrey; Emily N Chin; Alexandra E Porter; Kristin Butcher; Robert O Ritchie; Richard A Schneider; Anil Lalwani; Rik Derynck; Grayson W Marshall; Sally J Marshall; Lawrence Lustig; Tamara Alliston
Journal:  EMBO Rep       Date:  2010-09-17       Impact factor: 8.807

3.  Skeletal Dysplasia Presenting as a Neuromuscular Disorder - Report of a Family with Camurati-Engelmann Syndrome.

Authors:  Vasilica Plaiasu; Amalia Costin
Journal:  Maedica (Buchar)       Date:  2015-03

4.  Camurati-Engelmann disease: unique variant featuring a novel mutation in TGFβ1 encoding transforming growth factor beta 1 and a missense change in TNFSF11 encoding RANK ligand.

Authors:  Michael P Whyte; William G Totty; Deborah V Novack; Xiafang Zhang; Deborah Wenkert; Steven Mumm
Journal:  J Bone Miner Res       Date:  2011-05       Impact factor: 6.741

5.  Clinical characteristics and treatment outcomes in Camurati-Engelmann disease: A case series.

Authors:  Yoon-Myung Kim; Eungu Kang; Jin-Ho Choi; Gu-Hwan Kim; Han-Wook Yoo; Beom Hee Lee
Journal:  Medicine (Baltimore)       Date:  2018-04       Impact factor: 1.889

6.  Visual and otologic manifestation of Camurati-Engelmann's disease: a case report.

Authors:  Tariq Alam; Muhammad Khurram; Hidayatullah Hamidi; Asif Alam Khan
Journal:  Radiol Case Rep       Date:  2015-10-09
  6 in total

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