Managing infants with craniofacial malformations - Where to go next?
Semin Fetal Neonatal Med
; 26(6): 101289, 2021 12.
Article
en En
| MEDLINE
| ID: mdl-34548245
ABSTRACT
Treatment of infants with craniofacial malformations, e.g. Robin sequence, is characterized by considerable heterogeneity and a lack of randomized trials to identify an optimal approach. We propose to establish an international register using a common minimal dataset that will better allow for a comparison between key determinants and outcomes in these patients. In infants, this should include an assessment of mandibular micrognathia, glossoptosis, upper airway obstruction, weight gain and mode of feeding. Later on, neurocognition, speech development, hearing and quality of life should also be included. Together, these data will help better to advice parents on which treatment to choose for their baby with a craniofacial malformation.
Texto completo:
1
Bases de datos:
MEDLINE
Asunto principal:
Síndrome de Pierre Robin
/
Obstrucción de las Vías Aéreas
Tipo de estudio:
Clinical_trials
Límite:
Humans
/
Infant
Idioma:
En
Revista:
Semin Fetal Neonatal Med
Asunto de la revista:
PEDIATRIA
/
PERINATOLOGIA
Año:
2021
Tipo del documento:
Article