Health-related quality of life in children and adolescents with syndromic craniosynostosis
Author:
Publisher
Elsevier BV
Subject
Surgery
Reference21 articles.
1. Mutation screening in patients with syndromic craniosynostoses indicates that a limited number of recurrent FGFR2 mutations accounts for severe forms of Pfeiffer syndrome;Lajeunie;Eur J Hum Genet,2006
2. Saethre-Chotzen syndrome caused by TWIST 1 gene mutations: functional differentiation from Muenke coronal synostosis syndrome;Kress;Eur J Hum Genet,2006
3. The origin of EFNB1 mutations in craniofrontonasal syndrome: frequent somatic mosaicism and explanation of the paucity of carrier males;Twigg;Am J Hum Genet,2006
4. Long-term functional outcome in 167 patients with syndromic craniosynostosis; defining a syndrome-specific risk profile;de Jong;J Plast Reconstr Aesthet Surg,2009
5. Reliability and validity of the Infant and Toddler Quality of Life Questionnaire (ITQOL) in a general population and respiratory disease sample;Raat;Qual Life Res,2007
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1. Experiences of surgical complications and reoperations in nonsyndromic sagittal synostosis patients in Oulu;Child's Nervous System;2024-06-28
2. Prospective Evaluation of Health-Related Quality-of-Life in Children with Craniosynostosis;The Cleft Palate Craniofacial Journal;2024-02-21
3. What We Know About Intracranial Hypertension in Children With Syndromic Craniosynostosis;Journal of Craniofacial Surgery;2023-07-24
4. Craniosynostosis in Patients With X‐Linked Hypophosphatemia: A Review;JBMR Plus;2023-03-14
5. Increased utilization of healthcare services in children with craniosynostosis;Journal of Neurosurgery: Pediatrics;2022-07-01
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