Scholar : Ειδοποίηση Μελετητή - [ Laryngomal

Ειδοποίηση Μελετητή:[ Laryngomalacia ]

[HTML] Autosomal recessive cutis laxa Type II: Report of novel mutation in a child

R Kumar, S Sharda, V Soni, K Nambiyar - Indian Dermatology Online Journal, 2017

... Case Report, Top. A 14-month-old boy presented with predominant motor developmental delay
and seizures. Child also had stridor and indirect laryngoscopy suggested laryngomalacia. ...
Laryngomalacia and inspiratory stridor settled slowly by 2 ½ years. ...

[HTML] Swallowing Disorders in Newborn and Small Children

D Farneti, E Genovese - Advances in Speech-language Pathology, 2017

... affecting neuromuscular coordination (prematurity and low birth weight), complex diseases (heart
disease, lung disease, gastroesophageal reflux disease, and delayed gastric emptying), structural
anomalies (cleft lip and/or palate, laryngomalacia, tracheoesophageal fistula ...

[PDF] AN INVESTIGATION OF RESPIRATORY RESISTANCE DURING RESTING BREATHING IN TEENAGE FEMALE ATHLETES WITH AND WITHOUT PARADOXICAL …

AL Pham - 2017

... what constitutes PVFMD should not be confused with other disorders that cause
airway obstruction, such as laryngomalacia, papillomatosis, vocal fold paralysis,
and laryngeal webbing (Sandage & Zelazny, 2004). Differences ...

Expanding the clinical and molecular spectrum of PRMT7 mutations: three additional patients and review

E Agolini, ML Dentici, E Bellacchio, V Alesi, FC Radio… - Clinical Genetics

... Ocular anomalies Blue sclerae no coloboma strabismus strabismus strabismus no
dacryostenosis no strabismus 7/10 (70%) Laryngomalacia NK NK NK NK NK NK yes yes no
no 2/4 (50%) Cryptorchidism NA NA NA NA NA NA yes no yes NA 2/3 (67%) ...

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