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Congenital high airway obstruction syndrome: prenatal ultrasound diagnosis and literature review
Author(s) -
Bashiru Babatunde Jimah,
Teresa Aba Mensah,
Kofi Appiah,
Benjamin Dabo Sarkodie,
Edwin Gwira Tamattey,
Dorothea Anim
Publication year - 2020
Publication title -
health sciences investigations journal
Language(s) - English
Resource type - Journals
eISSN - 2720-7609
pISSN - 2704-4890
DOI - 10.46829/hsijournal.2020.12.1.2.144-148
Subject(s) - medicine , polyhydramnios , airway obstruction , larynx , in utero , prenatal diagnosis , prenatal ultrasound , airway , atresia , stenosis , lesion , surgery , pregnancy , radiology , fetus , genetics , biology
Congenital high airway obstruction syndrome (CHAOS) is a rare congenital anomaly involving the upper airways (trachea, larynx). It is a life-threatening condition whose true incidence is unknown. The obstruction may be due to tracheal/laryngeal atresia, stenosis, or the presence of a mass lesion. Prognosis is poor, generally resulting in stillbirth or intrauterine fetal demise. Ex utero intrapartum treatment (EXIT) is possible if the condition is detected early. We present a case of CHAOS diagnosed during a second-trimester anomaly scan with postmortem confirmation and literature review.

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