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.
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N. Fourla et al. · 2022 · Journal of Surgical Case Reports
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2022 · Journal of Surgical Case Reports
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Saranya Thangavel et al. · 2021 · BMJ Case Reports
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2021 · BMJ Case Reports
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Yuli Tetriana Sari et al. · 2019 ·
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2017 · Journal of Otolaryngology Advances
A sample of recent works citing this journal's research on Congenital Arhinia, linking to each citing work.