Dental Appliances for the treatment of obstructive sleep apnea in children: a systematic review and Meta-analysis

D Marciuc, S Morarasu, BC Morarasu, EA Marciuc… - Medicina, 2023 - mdpi.com
Background and objectives: Obstructive sleep apnea (OSA) in children is a debilitating
disease, difficult to treat. Dental appliances have been proposed as a valid therapy for …

Syndromic craniofacial disorders

RJ Tibesar, AR Scott - Facial Plastic Surgery Clinics, 2024 - facialplastic.theclinics.com
It is estimated that there are more than 500 syndromes that present with craniofacial
anomalies. 1 The 2 major categories of craniofacial syndromes are those associated with …

Incidence of non-syndromic and syndromic craniosynostosis in Sweden

P Tarnow, L Kölby, G Maltese… - Journal of …, 2022 - journals.lww.com
Premature craniosynostosis is a rare condition, with a wide range of incidence estimations in
the literature. The aim of this study was to establish the current incidence among the …

Outcomes after endoscope-assisted strip craniectomy and orthotic therapy for syndromic craniosynostosis

SN Chiang, GB Skolnick, SD Naidoo… - Plastic and …, 2023 - journals.lww.com
Background: Endoscopic craniosynostosis repair has emerged as an effective alternative to
open repair, but data are limited on treatment of the 15% to 24% of patients with syndromic …

Mechanical loading of cranial joints minimizes the craniofacial phenotype in Crouzon syndrome

M Moazen, M Hejazi, D Savery, D Jones… - Scientific Reports, 2022 - nature.com
Children with syndromic forms of craniosynostosis undergo a plethora of surgical
interventions to resolve the clinical features caused by the premature fusion of cranial …

Quality of life in patients with craniosynostosis and deformational plagiocephaly: a systematic review

KM Park, NV Tripathi, F Al-Mufarrej - International Journal of Pediatric …, 2021 - Elsevier
Background Craniosynostosis is a bony dysmorphism of the calvarium due to premature
suture fusion and is classified as syndromic (part of congenital syndrome) or nonsyndromic …

Genetic bases of craniosynostoses: An update

T Armand, E Schaefer, F Di Rocco, P Edery, C Collet… - Neurochirurgie, 2019 - Elsevier
Craniosynostosis (CS) is defined as the premature fusion of cranial sutures, leading to an
abnormal skull shape. The overall incidence is between 1: 2,000 and 1: 3,000 live births …

Crouzon syndrome and the eye: An overview

K Bhattacharjee, O Rehman… - Indian Journal of …, 2022 - journals.lww.com
The current literature review aims to evaluate the ocular findings and associated ophthalmic
features in Crouzon syndrome. Craniosynostoses are syndromes characterized by …

Craniofacial morphology in Apert syndrome: A systematic review and meta-analysis

MK Alam, AA Alfawzan, KC Srivastava, D Shrivastava… - Scientific reports, 2022 - nature.com
This meta-analysis aims to compare Apert syndrome (AS) patients with non-AS populations
(not clinically or genetically diagnosed) on craniofacial cephalometric characteristics (CCC) …

[HTML][HTML] Sensitivity, Specificity, and Cutoff Identifying Optic Atrophy by Macular Ganglion Cell Layer Volume in Syndromic Craniosynostosis

YH Chang, SJ Staffa, LY Saricay, D Zurakowski, R Gise… - Ophthalmology, 2024 - Elsevier
Purpose To determine the sensitivity, specificity, and cutoff of macular ganglion cell layer
(GCL) volume consistent with optic atrophy in children with syndromic craniosynostosis and …