Literature DB >> 11981393

Three familial cases of Michel's aplasia.

Ahmad Daneshi1, Mohammad Farhadi, Alimohamad Asghari, Hesamedin Emamjomeh, Parvaneh Abbasalipour, Saeed Hasanzadeh.   

Abstract

Complete agenesis of the bony labyrinth, first described by Michel, represents the most severe form of inner ear defect. A search of the literature yielded only one report of this rare anomaly, affecting two siblings. Three familial cases of bilateral inner ear aplasia are reported here, and the probable inheritance pattern of this condition is discussed.

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Year:  2002        PMID: 11981393     DOI: 10.1097/00129492-200205000-00020

Source DB:  PubMed          Journal:  Otol Neurotol        ISSN: 1531-7129            Impact factor:   2.311


  4 in total

1.  What is expected of the facial nerve in michel aplasia? Anatomic variation.

Authors:  Masoud Motasaddi Zarandy; Ali Kouhi; Shervin Sharif Kashany; Sohrab Rabiei; Fatemeh Hajimohamadi; Mahtab Rabbani-Anari
Journal:  Skull Base       Date:  2010-11

2.  Variable expressivity of FGF3 mutations associated with deafness and LAMM syndrome.

Authors:  Saima Riazuddin; Zubair M Ahmed; Rashmi S Hegde; Shaheen N Khan; Idrees Nasir; Uzma Shaukat; Sheikh Riazuddin; John A Butman; Andrew J Griffith; Thomas B Friedman; Byung Yoon Choi
Journal:  BMC Med Genet       Date:  2011-02-09       Impact factor: 2.103

3.  From labyrinthine aplasia to otocyst deformity.

Authors:  Anja Maria Giesemann; Friedrich Goetz; Jürgen Neuburger; Thomas Lenarz; Heinrich Lanfermann
Journal:  Neuroradiology       Date:  2009-10-02       Impact factor: 2.804

4.  Complete Labyrinthine Aplasia: A Unique Sign for Targeted Genetic Testing in Hearing Loss.

Authors:  Meenakshi Lallar; Veronica Arora; Renu Saxena; Ratna Dua Puri; Ishwar Chander Verma
Journal:  J Pediatr Genet       Date:  2020-03-09
  4 in total

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