Publication date: May 2017
Source:International Journal of Pediatric Otorhinolaryngology, Volume 96
Author(s): Rosalba Sacca, Karen B. Zur, T. Blaine Crowley, Elaine H. Zackai, Kathleen D. Valverde, Donna M. McDonald-McGinn
Introduction22q11.2 deletion syndrome (22q11.2DS) presents with complex but variable symptoms, including cardiac, immune, palatal, endocrine, cognitive, and psychiatric issues. However, an association of 22q11.2DS with structural airway abnormalities has not been formally described. The aim of this study was to document the frequency of this association.MethodsWe retrospectively reviewed medical records of patients with 22q11.2DS evaluated in the 22q and You Center at the Children's Hospital of Philadelphia between 1999 and 2015 referred to otolaryngology for an airway assessment. Type of airway abnormality and presence of comorbidities, such as congenital heart disease, tracheostomy, and association with prenatal symptomatology such as polyhydramnios, were noted.ResultsOf the 104 patients who underwent an otolaryngology procedure (microlaryngoscopy or bronchoscopy), 71% (n = 74) had airway abnormalities. Patients with airway abnormalities ranged in age from 5 months to 37 years, with similar prevalence among males and females. Observed airway abnormalities included tracheomalacia (36%), subglottic stenosis (28%), laryngomalacia (26%), glottic web (21%), and bronchomalacia (16%). Most patients with airway abnormalities (91%) had an associated congenital heart defect, with ventricular septal defect and Tetralogy of Fallot being the most prevalent. Importantly, 30% of patients required a tracheostomy, and overall polyhydramnios was noted in 16% of pregnancies.ConclusionAirway abnormalities are a common feature of 22q11.2DS, leading to substantial morbidity, particularly when combined with complex cardiac disease. Polyhydramnios may be an important prenatal clue to both the diagnosis of 22q11.2DS and airway anomalies. Postnatal assessment of airway structure and function among patients with 22q11.2DS is an important component of overall evaluation and will help guide long-term management.
http://ift.tt/2mQPrDe
Σφακιανάκης Αλέξανδρος
ΩτοΡινοΛαρυγγολόγος
Αναπαύσεως 5 Άγιος Νικόλαος
Κρήτη 72100
00302841026182
00306932607174
alsfakia@gmail.com
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Δευτέρα 6 Μαρτίου 2017
Association of airway abnormalities with 22q11.2 deletion syndrome
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- Medial Olivocochlear function in children with poo...
- Association of airway abnormalities with 22q11.2 d...
- Reliability and validity of the Dutch pediatric Vo...
- Management of orbital cellulitis and subperiosteal...
- Coblation of suprastomal granulomas in tracheostom...
- Five-years’ experience with outpatient thyroglossa...
- The Analysis of Reliability and Validity of the IT...
- Peri-operative management of high-risk paediatric ...
- MYO15A splicing mutations in hearing loss: A revie...
- The public health resource utilization impact of a...
- Theory of mind and language development in Japanes...
- Using sildenafil (viagra) to treat congenital lymp...
- No catheter angiography is needed in patients with...
- Fluorocholine PET/CT predicts skeletal progression...
- Robust detection and segmentation of cell nuclei i...
- Impact of osteopathic therapy on pro-prioceptive b...
- The Rebound Boots Change the Lower Limb Muscle Act...
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- Dermoscopic appearance of hair casts
- Relapsing polychondritis associated with psoriasis...
- Prognosis of adult-onset clinically amyopathic der...
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