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Titre : | Sleep frequently asked questions: Question 1 : what abnormalities do babies with cleft lip and/or palate have on polysomnography? (2019) |
Auteurs : | Joanna E. MacLean |
Type de document : | Article |
Dans : | Midwifery Digest (Midirs) (Vol. 29, n° 1, March 2019) |
Article en page(s) : | p. 107-111 |
Langues: | Anglais |
Descripteurs : |
HE Vinci Aberrations des chromosomes ; Bec-de-lièvre ; Fente labiopalatine ; Malformations ; Nourrisson ; Polysomnographie ; Respiration ; Sommeil |
Résumé : |
Cleft lip and/or palate (CL/P) is one of the most common congenital malformations with an estimated birth prevalence world wide of 12.44 (95% CI 9.7215.93) per 10,000 births for naturally conceived singleton births; prevalence is higher in infants conceived using assisted reproductive technologies [1]. CL/P can occur in isolation or with other anomalies or chromosomal variations and are classified as non-syndromic and syndromic CL/P based on the absence or presence of other congenital anomalies [2]; approximately 2/3rd of CL/P occurs in isolation or as nonsyndromic CL/P and 1/3rd as syndromic [3]. CL/P includes a spectrum of clefts of the primary palate (cleft lip and alveolus) and secondary palate (hard and soft palate) and can be incomplete or complete as well as unilateral or bilateral, and subclinical [4]. Palatal clefts also differ in shape with a characteristic U-shaped cleft associated with Robin sequence in contrast to a typical V-shaped in non-syndromic CL/P. The prevalence, type, and severity of CL/P differ by ethnicity, country, regions, and sex with both genetic and environment factors implicated in the aetiology of CL/P [1,2,4]. Associated anomalies as well as cleft type determine the overall presentation of an infant with CL/P including associated respiratory impairments.
Respiratory impairments, |
Disponible en ligne : | Non |
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REV | Périodique papier | Woluwe | Espace revues | Consultation sur place uniquement Exclu du prêt |