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Tracheal Stenosis and Congenital Heart Disease in Trisomy 21

Bibliographic Data

ID15714968
AuthorsRanjit I Kylat (0000-0001-9666-6883, University of Arizona, corresponding author)
Year2019
Volume6
Issue9
Pages98-98
Publication date2019-09-04
Open AccessYes
TypeARTICLE
VenueChildren (JOURNAL)
Journal identifiersISSN: 2227-9067 • E-ISSN: 2227-9067
PublisherMultidisciplinary Digital Publishing Institute (PUBLISHER • CH)
DOI10.3390/children6090098
PMID31487969
OpenAlexW2971518300
LanguageEN
References cited16

Tracheal rings (TR) are rare, congenital cartilaginous defect of the upper airway and are usually due to complete or near complete circumferential cartilaginous tracheal rings, with variable degrees of tracheal stenosis (TS) and shortening. Chromosomal anomalies like trisomy 21 are characteristically associated with a wide range of upper airway anomalies including TS and congenital heart disease (CHD). However, the overall prevalence of severe forms of TS is rare and reported in 1.2% of all CHD patients. Herein, we present a rare association of severe TS due to complete tracheal rings in a trisomy 21 patient with CHD and the challenges in the management

Airway · Biology · Cardiology · Disease · Heart disease · Rare disease · Stenosis · Tracheal Stenosis · Trisomy · Congenital Diaphragmatic Hernia Studies · Medicine · Tracheal and airway disorders · Tumors and Oncological Cases · Genetics · Internal Medicine · Surgery

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