www.fgks.org   »   [go: up one dir, main page]

Inner ear anomalies are frequent but nonobligatory features of the branchio-oto-renal syndrome

Arch Otolaryngol Head Neck Surg. 2002 Sep;128(9):1033-8. doi: 10.1001/archotol.128.9.1033.

Abstract

Objective: To summarize the syndromic features and evaluate the presence of inner ear anomalies in 35 patients with branchio-oto-renal (BOR) syndrome from 6 families.

Design: Retrospective evaluation of magnetic resonance imaging of the temporal bones and clinical features in patients with BOR syndrome.

Setting: Tertiary referral center.

Patients: The study population comprised 35 clinically affected patients with BOR syndrome from 6 families. Most of these families were followed for over 25 years.

Main outcome measures: Twenty-four patients underwent high-resolution, heavily T2-weighted 3-dimensional magnetic resonance imaging of the temporal bones for evaluation of inner ear anomalies. Special attention was paid to the endolymphatic duct and sac.

Results: A total of 7 enlarged endolymphatic ducts and sacs (3 bilaterally and 4 unilaterally) and 5 enlarged endolymphatic ducts only (2 bilaterally and 3 unilaterally) were observed. Eight hypoplastic cochleas and 6 hypoplastic labyrinths were seen bilaterally. Seven family members had normal inner ears.

Conclusion: These findings suggest that inner ear anomalies are frequent but nonobligatory features of BOR syndrome.

Publication types

  • Research Support, Non-U.S. Gov't
  • Research Support, U.S. Gov't, P.H.S.

MeSH terms

  • Adult
  • Branchio-Oto-Renal Syndrome / genetics
  • Branchio-Oto-Renal Syndrome / pathology*
  • Child
  • Ear, Inner / abnormalities*
  • Ear, Inner / pathology*
  • Female
  • Follow-Up Studies
  • Humans
  • Magnetic Resonance Imaging
  • Male
  • Pedigree
  • Retrospective Studies
  • Temporal Bone / abnormalities
  • Temporal Bone / pathology
  • Time Factors