Three familial cases of Michel's aplasia

Otol Neurotol. 2002 May;23(3):346-8. doi: 10.1097/00129492-200205000-00020.

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.

Publication types

  • Case Reports

MeSH terms

  • Child
  • Child, Preschool
  • Ear, Inner / abnormalities*
  • Ear, Inner / diagnostic imaging*
  • Female
  • Genetic Diseases, Inborn / complications
  • Genetic Diseases, Inborn / diagnostic imaging*
  • Genetic Diseases, Inborn / rehabilitation
  • Hearing Loss, Sensorineural / etiology
  • Humans
  • Male
  • Pedigree
  • Tomography, X-Ray Computed