Literature DB >> 24469189

Patient-reported quality of life in highest-functioning Apert and Crouzon syndromes: a comparative study.

Cassio Eduardo Raposo-Amaral1, José Garcia Junqueira Neto, Rafael Denadai, Cassio Menezes Raposo-Amaral, Cesar Augusto Raposo-Amaral.   

Abstract

BACKGROUND: Crouzon and Apert syndromes are the most common syndromic forms of craniofacial dysostosis. Apert syndrome has a broad clinical spectrum, including complex craniofacial involvement, as well as limiting deformities of the hands, feet, and other joints that require multiple surgical procedures when compared with Crouzon syndrome, which is generally less severe. The authors hypothesized that the quality of life of Apert syndrome patients is inferior to that of Crouzon syndrome patients.
METHODS: The quality of life of Apert (n = 8) and Crouzon (n = 12) syndrome patients was assessed using the World Health Organization Quality of Life-100 questionnaire. The Mann-Whitney test was used to compare the quality-of-life scores between Apert and Crouzon patients. Values were considered significant for a confidence interval of 95 percent (p < 0.05).
RESULTS: Apert patients showed an overall higher (score > 60 percent) quality of life in most World Health Organization Quality of Life-100 facets (68 percent) and domains (83.33 percent), with significance (p < 0.05) in three facets (energy and fatigue, mobility, and environment in the home), compared with Crouzon patients.
CONCLUSION: Contrary to the authors' initial hypothesis, both the highest-functioning Apert patients and the Crouzon patients presented a satisfactory quality of life, demonstrating that these syndromic patients had acquired the necessary repertoire to manage the adverse daily situations of their lives.

Entities:  

Mesh:

Year:  2014        PMID: 24469189     DOI: 10.1097/01.prs.0000437260.31693.75

Source DB:  PubMed          Journal:  Plast Reconstr Surg        ISSN: 0032-1052            Impact factor:   4.730


  5 in total

Review 1.  Syndromic Craniosynostosis: Complexities of Clinical Care.

Authors:  Justine O'Hara; Federica Ruggiero; Louise Wilson; Greg James; Graeme Glass; Owase Jeelani; Juling Ong; Richard Bowman; Michelle Wyatt; Robert Evans; Martin Samuels; Richard Hayward; David J Dunaway
Journal:  Mol Syndromol       Date:  2019-01-16

2.  Hand Function in Apert Syndrome.

Authors:  Cassio Eduardo Raposo-Amaral; Rafael Denadai; Thais Miguel do Monte Lameiro; Yuri Moresco de Oliveira; Cesar Augusto Raposo-Amaral
Journal:  Plast Reconstr Surg Glob Open       Date:  2019-05-01

3.  Detection of G338R FGFR2 mutation in a Vietnamese patient with Crouzon syndrome.

Authors:  Anh Lan Thi Luong; Thuong Thi Ho; Ha Hoang; Trung Quang Nguyen; Tu Cam Ho; Phan Duc Tran; Thuy Thi Hoang; Nam Trung Nguyen; Hoang Ha Chu
Journal:  Biomed Rep       Date:  2019-01-03

Review 4.  Diagnosis of infant synostotic and nonsynostotic cranial deformities: a review for pediatricians.

Authors:  Enrico Ghizoni; Rafael Denadai; Cesar Augusto Raposo-Amaral; Andrei Fernandes Joaquim; Helder Tedeschi; Cassio Eduardo Raposo-Amaral
Journal:  Rev Paul Pediatr       Date:  2016-05-12

5.  Clinical study and some molecular features of Mexican patients with syndromic craniosynostosis.

Authors:  Aurora Ibarra-Arce; Manuel Almaraz-Salinas; Víctor Martínez-Rosas; Gabriela Ortiz de Zárate-Alarcón; Laura Flores-Peña; Mirza Romero-Valdovinos; Angélica Olivo-Díaz
Journal:  Mol Genet Genomic Med       Date:  2020-06-08       Impact factor: 2.183

  5 in total

北京卡尤迪生物科技股份有限公司 © 2022-2023.