A Case Report of Aquired Choanal Atresia

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Case Report Congenital Bilateral Choanal Atresia

Congenital choanal atresia (CCA) is the developmental failure of the nasal cavity to communicate with nasopharynx. Surgical repair is recommended in the first weeks of life in bilateral cases because this is a lifethreatening situation in newborns. This is a case report of a full term, healthy newborn baby presenting with intermittent attacks of cyanosis and respiratory distress soon after birt...

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Association of Nasal Nostril Stenosis with Bilateral Choanal Atresia: A Case Report

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Unilateral choanal atresia in one monozygotic twin: a case report.

Unilateral atresia is an extremely uncommon congenital disorder in monozygotic twins. We present the first case in the literature of premature, monozygotic twins with no other congenital genetic defects other than only one twin with unilateral choanal atresia on the right side, being the other sibling completely normal. Diagnostic examinations performed to both twins consisted of nasal endoscop...

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Congenital Bilateral Choanal Atresia: A Rare Case

Congenital Choanal Atresia (CCA) is the developmental misstep or inadequacy of the nasal cavity to connect posteriorly with the nasopharynx. Bilateral atresia presents with life threatening asphyxia at birth, while unilateral variety often remains unnoticed and presents later. This is to highlight the importance of taking into account the bilateral form in differential diagnosis of severe respi...

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Choanal atresia.

Choanal atresia is caused by failure of resorption of the bucco-pharyngeal membrane during embryonic development. The atresia can be membranous or bony in nature, but is usually mixed in most cases. When the atresia is bilateral, newborns can have severe airway distress and cyanosis is alleviated by crying. Bilateral choanal atresia is managed with an oropharyngeal airway. Flexible nasal endosc...

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ژورنال

عنوان ژورنال: Practica oto-rhino-laryngologica. Suppl.

سال: 1988

ISSN: 0912-1870

DOI: 10.5631/jibirinsuppl1986.1988.supplement25_93