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Congenital Arhinia: A Rare Case Report and Review of Literature

  • Uttam Mondal
  • Rameshwar PrasadEmail author
Clinical Report
  • 71 Downloads

Abstract

Congenital absence of nose (Arhinia) is extremely rare. A male baby was born at term via uncomplicated vaginal delivery and presented with complete arhinia, bilateral microphthalmia, lower eyelid coloboma and feeding difficulty. Reconstructive surgery was postponed until preschool age. On follow up at 1 year of age baby is feeding liquid and semisolid food and growing well.

Keywords

Arhinia Microphthalmia Coloboma Congenital anomaly 

Notes

Author’s Contribution

Dr. Uttam Mondal: Diagnosis, work up and management of the case, Dr. Rameshwar Prasad: management and follow up of the case, review of literature and preparation of final manuscript.

Compliance with Ethical Standards

Conflict of interest

Dr. Uttam Mondal declares that he has no conflict of interest. Dr. Rameshwar Prasad declares that he has no conflict of interest.

Ethical Approval

This article does not contain any studies with human participants or animals performed by any of the authors.

Informed Consent

Informed consent was obtained from all individual participants included in the study.

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Copyright information

© Association of Otolaryngologists of India 2016

Authors and Affiliations

  1. 1.Department of NeonatologyIPGME&R and SSKM HospitalKolkataIndia

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