Literature DB >> 29287846

Congenital respiratory tract disorders in 22q11.2 deletion syndrome.

Emmy Verheij1, Lucienne Speleman2, Aebele B Mink van der Molen3, Henricus G X M Thomeer4.   

Abstract

OBJECTIVE: Respiratory tract disorders have been reported in patients with 22q11.2 deletion syndrome, however infrequently. This study describes the respiratory tract disorders encountered in a cohort of 278 patients with 22q11.2 deletion syndrome.
METHODS: We conducted a retrospective, cross-sectional, study at a single tertiary referral center. We identified the patients with 22q11.2 deletion syndrome and with an upper and/or lower respiratory tract disorder at our otorhinolaryngologic department. The different disorders were described.
RESULTS: Out of 278 patients referred to the otorhinolaryngologic department, we identified 14 patients with a laryngeal and/or tracheal disorder. Nine patients had more than one congenital disorder in this anatomical area. Disorders included a choanal stenosis (n = 1), laryngeal web (n = 5), laryngeal cleft (n = 2), subglottic stenosis (n = 3), pharyngo-, laryngo-, tracheo- and/or bronchomalacia (n = 11) and tracheal stenosis (n = 1).
CONCLUSION: Different types of respiratory tract disorders can be present in patients with 22q11.2 deletion syndrome. Clinicians should be aware of this clinical association for timely and accurate diagnosis and treatment. In addition, the diagnosis 22q11.2 deletion syndrome should be considered in patients presenting with a congenital respiratory tract disorder.
Copyright © 2017 Elsevier B.V. All rights reserved.

Entities:  

Keywords:  22q11 deletion; Airway malacia; DiGeorge syndrome; Laryngeal web; Subglottic stenosis; Velocardiofacial syndrome

Mesh:

Year:  2017        PMID: 29287846     DOI: 10.1016/j.ijporl.2017.10.028

Source DB:  PubMed          Journal:  Int J Pediatr Otorhinolaryngol        ISSN: 0165-5876            Impact factor:   1.675


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