Congenital Bilateral Choanal Atresia: A Rare Case

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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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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 life-threatening 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 bir...

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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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Yenido¤anlar hayatlar›n›n ilk birkaç ay›nda zorunlu olarak burundan nefes al›rlar. Yenido¤anda bilateral konjenital atrezi; düzensiz nefes alma, intermittan siyanoz, a¤lama ile semptomlar›n düzelmesi, beslenme ile respiratuvar s›k›nt›n›n artmas› ve bazen neonatal asfiksiye ba¤l› ölümlere neden olmas› dolay›s› ile acil bir durumdur. Fark edilmeden yetiflkin döneme kadar ulaflabilen konjenital bi...

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ژورنال

عنوان ژورنال: Journal of Rare Disorders: Diagnosis & Therapy

سال: 2018

ISSN: 2380-7245

DOI: 10.21767/2380-7245.100162