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, 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.

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Related Articles

7 article(s) found

Prenatal Prognostication of Congenital Diaphragmatic Hernia: What are we Looking at?

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Single Daily Activity or Exercise Capacity Measurements Did not Predict Future Changes in Cardiovascular Risk Factors in Congenital Heart Disease

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Title - Case of Unilateral Congenital Aural Atresia & Microtia with Cholesteatoma

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Reproductive Performance and Factors Influencing Fetal Outcome: A Practical Guide to Experiments on Lung Development in A Nitro Fen-Induced Rat Model for Congenital Diaphragmatic Hernia

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Resolution of Fetal Hydrops in a Case of Congenital Pulmonary Airway Malformation

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Prevalence of Congenital Heart Defects among Neonates in Port Harcourt, Rivers State, Nigeria

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Correlations with Congenital Syphilis in the United States: A Cross-Sectional Study

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