Skip to main content

Advertisement

Log in

Cochlear Implantation in Pierre Robin Syndrome

  • Clinical Report
  • Published:
Indian Journal of Otolaryngology and Head & Neck Surgery Aims and scope Submit manuscript

Abstract

Hereditary hearing loss accounts for nearly 60% of deafness in developed countries and about 30% of them are syndromic. Pierre Robin Syndrome is one such condition. The patient with this syndrome usually presnts with triad of micrognathia, glossoptosis and cleft palate. Hearing loss is mostly conductive but there can be sensorineural hearing loss also. Here we present a case of Pierre Robin Syndrome who presented with congenital hearing loss. He also had bilateral serous otitis media. He underwent cochlear implant surgery and was prescribed antihistaminics and steroid spray for middle ear effusion. Therefore, proper clinical evaluation is required.

This is a preview of subscription content, log in via an institution to check access.

Access this article

Price excludes VAT (USA)
Tax calculation will be finalised during checkout.

Instant access to the full article PDF.

Fig. 1
Fig. 2

Similar content being viewed by others

References

  1. Barlow-Stewart K, Mona Sale (2007) Centre for genetics education. Deafness and hearing loss–genetic aspects. The Australasian genetics Resource Book.

  2. Berrettini S (2008) Linee guida per la conduzione dello screening audiologico neonatale nella regione Toscana http://www.fimp.org

  3. Evans KN, Sie KC, Hopper RA, Glass RP, Hing AV, Cunningham ML (2011) Robin sequence: from diagnosis to development of an effective management plan. Pediatr 127(5):936–948

    Article  Google Scholar 

  4. Breugem CC, Evans KN, Poets CF, Suri S, Picard A, Filip C et al (2016) Best practices for the diagnosis and evaluation of infants with robin sequence: a clinical consensus report. JAMA Pediatr 170:894–902. https://doi.org/10.1001/jamapediatrics.2016.0796

    Article  PubMed  Google Scholar 

  5. Handzić J, Bagatin M, Subotić R, Cuk V (1995) Hearing levels in pierre robin syndrome. Cleft Palate Craniofac J 32(1):30–36

    Article  Google Scholar 

  6. Medard C, François M, Narcy P (1999) Hearing status of robin sequence patients. Ann Otolaryngol Chir Cervicofac 116(6):317–321

    CAS  PubMed  Google Scholar 

  7. Sando I, Takahashi H (1990) Otitis media in association with various congenital diseases; preliminary study. Ann Otol Rhinol Laryngol 99:13–16

    Article  Google Scholar 

  8. Gruen PM, Carranza A, Karmody CS, Bachor E (2005) Anomalies of the ear in the pierre robin triad. Ann Otol Rhinol Laryngol 114(8):605–613

    Article  Google Scholar 

  9. Igarashi M, Filippone MV, Alford BR (1976) Temporal bone findings in pierre robin`. Laryngoscope 86:1679–1687. https://doi.org/10.1288/00005537-197611000-00009

    Article  CAS  PubMed  Google Scholar 

Download references

Author information

Authors and Affiliations

Authors

Corresponding author

Correspondence to Mohnish Grover.

Additional information

Publisher's Note

Springer Nature remains neutral with regard to jurisdictional claims in published maps and institutional affiliations.

Rights and permissions

Reprints and permissions

About this article

Check for updates. Verify currency and authenticity via CrossMark

Cite this article

Gupta, S., Dagur, M., Grover, M. et al. Cochlear Implantation in Pierre Robin Syndrome. Indian J Otolaryngol Head Neck Surg 73, 392–394 (2021). https://doi.org/10.1007/s12070-020-02331-9

Download citation

  • Received:

  • Accepted:

  • Published:

  • Issue Date:

  • DOI: https://doi.org/10.1007/s12070-020-02331-9

Keywords

Navigation