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==[[Choanal atresia overview|Overview]]==
==[[Choanal atresia overview|Overview]]==

Revision as of 17:10, 19 August 2020

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Overview

Choanal atresia is a congenital disorder where the back of the nasal passage is blocked, usually by abnormal bony or soft tissue.

Historical Perspective

Classification

Pathophysiology

Causes

Differentiating Choanal atresia from other Diseases

Epidemiology and Demographics

Risk Factors

Screening

Natural History, Complications and Prognosis

Diagnosis

History and Symptoms | Physical Examination | Laboratory Findings | Chest X Ray | CT | MRI | Other Imaging Findings | Other Diagnostic Studies

Presentation

It can be unilateral or bilateral.

Sometimes, a unilateral choanal atresia is not detected until much later in life because the baby manages to get along with only one nostril available for breathing.

Bilateral choanal atresia is a very serious life-threatening condition because the baby will then be unable to breathe directly after birth as babies are obligate nasal breathers (they must use their noses to breathe). These babies usually require airway resuscitation right after birth.

Treatment

The only possible treatment is surgery to correct the defect. [1]

See also

References

  1. Gosepath J, Santamaria VE, Lippert BM, Mann WJ (2007). "Forty-one cases of congenital choanal atresia over 26 years--retrospective analysis of outcome and technique". Rhinology. 45 (2): 158–63. PMID 17708465.


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