Laryngeal abnormalities are frequent in the 22q11 deletion syndrome

International Journal of Pediatric Otorhinolaryngology

Volumn 76, Issue 1, 2012, Pages 36-40

  Leopold, C ^a   De Barros, A ^a   Cellier, C ^a   Drouin Garraud, V ^a   Dehesdin, D ^a,b   Marie, J P ^a,b  

^a ROUEN UNIVERSITY HOSPITAL   (France)

^b CHU de Rouen   (France)

Author keywords

22q11 deletion; DiGeorge sequence; Larynx

Indexed keywords

ARTICLE; BRONCHIAL MALPOSITION; CHILD; CHROMOSOME DELETION 22Q11; CLINICAL ARTICLE; DISEASE ASSOCIATION; FEMALE; GLOTTIC WEB; HUMAN; INFANT; LARYNGOMALACIA; LARYNGOPLASTY; LARYNX DISORDER; LARYNX PARALYSIS; MALE; PRESCHOOL CHILD; PRIORITY JOURNAL; RETROSPECTIVE STUDY; SPEECH THERAPY; SUBGLOTTIC STENOSIS; VOCAL NODULE;

22Q11 DELETION SYNDROME; ABNORMALITIES, MULTIPLE; CHILD; COHORT STUDIES; COMBINED MODALITY THERAPY; DEVELOPMENTAL DISABILITIES; FEMALE; FOLLOW-UP STUDIES; HUMANS; INCIDENCE; INFANT, NEWBORN; INFANT, PREMATURE; LARYNGEAL DISEASES; LARYNGOSCOPY; LARYNX; MALE; RETROSPECTIVE STUDIES; SEVERITY OF ILLNESS INDEX;

EID: 84855527835     PISSN: 01655876     EISSN: 18728464     Source Type: Journal    
DOI: 10.1016/j.ijporl.2011.09.025     Document Type: Article

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