G452 (P) A complex case of cystic fibrosis and coffin-siris syndrome
E Weir, A Devenny, P Davies - 2018
… On newborn screening, identified as having CF (Delta F508/3849+10kbC
>T) but pancreatic sufficient. Respiratory polysomnography confirmed partial
obstruction with mixed events and microlaryngoscopy and bronchoscopy
>T) but pancreatic sufficient. Respiratory polysomnography confirmed partial
obstruction with mixed events and microlaryngoscopy and bronchoscopy
Congenital and iatrogenic laryngeal and vocal abnormalities in patients with 22q11. 2 deletion
B Ebert, J Sidman, N Morrell, BB Roby - International Journal of Pediatric …, 2018
… The major congenital abnormality was a laryngeal web (n = 10, 9.2%),
followed by subglottic stenosis (n = 7, 6.4% with 4 being congenital
subglottic stenosis), laryngeal cleft (n = 3, 2.8%), laryngomalacia (n = 1,
followed by subglottic stenosis (n = 7, 6.4% with 4 being congenital
subglottic stenosis), laryngeal cleft (n = 3, 2.8%), laryngomalacia (n = 1,
[PDF] Respiratory Infection in Children with Down Syndrome
RH Almaghrabi
… Laryngomalacia was the most common airway abnormality, with 50% incidence in the
DS group compared to 19% in the non-DS group. Tracheomalacia and tracheal bronchus,
and pulmonary hypoplasia have also been reported in DS children [46,47] …
DS group compared to 19% in the non-DS group. Tracheomalacia and tracheal bronchus,
and pulmonary hypoplasia have also been reported in DS children [46,47] …
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