Research Topic · Peer-Reviewed

Congenital Arhinia

Congenital arhinia is a rare congenital disorder characterized by the absence of the nose and associated structures. The cause of this condition is unknown, but genetic and environmental factors may play a role. It most commonly manifests in infancy, but can occur at any age. Symptoms include difficulty nursing, dif…

Curated from this journal's research 📚 1 peer-reviewed article cited Cited 6× across the literature 🔖 ISSN 2379-8572 🗓 Reviewed July 2026

Overview

Congenital arhinia is a rare congenital disorder characterized by the absence of the nose and associated structures. The cause of this condition is unknown, but genetic and environmental factors may play a role. It most commonly manifests in infancy, but can occur at any age. Symptoms include difficulty nursing, difficulty breathing, and a widened nasal bridge. Treatment options are limited and typically involve reconstructive nasal surgery to restore nasal structure and improve breathing and cosmetic appearance. Congenital arhinia is a rare and serious condition which can have a significant impact on quality of life, however comprehensive care can help patients manage their symptoms and lead a full, healthy life.

Research published in this journal

1 peer-reviewed article, ranked by relevance. Each links to its DOI.

How this research is being cited

The 1 article above has been cited 6 times in the scholarly literature. Citation data via OpenAlex and Crossref, updated Jun 2026.

A sample of recent works citing this journal's research on Congenital Arhinia, linking to each citing work.

Editorial oversight

Curated from peer-reviewed research published in Otolaryngology Advances (ISSN 2379-8572).

Journal editorial board
Ioannis Chatzistefanou · Greece Heather Bortfeld · United States Heidi Silver · United States

This page summarises published research for orientation; it is not medical or professional advice.