Crouzon Syndrome: Basic Dysmorphology and Staging of Reconstruction

2019 ◽  
pp. 729-743
Author(s):  
Jeffrey C. Posnick
Keyword(s):  
Crouzon Syndrome

scholarly journals Characterization of dental pulp stem cells isolated from a patient diagnosed with Crouzon syndrome

2021 ◽  
Author(s):  
Daisuke Torii ◽  
Tomoko Kobayashi ◽  
Tetsuro Horie ◽  
Takeo W. Tsutsui
Keyword(s):  
Stem Cells ◽  
Dental Pulp ◽  
Dental Pulp Stem Cells ◽  
Crouzon Syndrome

Mutation associated with Crouzon syndrome causes ligand-independent dimerization and activation of FGF receptor-2

1997 ◽  
Vol 172 (1) ◽  
pp. 117-125 ◽  
Author(s):  
Karen Mangasarian ◽  
Yan Li ◽  
Alka Mansukhani ◽  
Claudio Basilico
Keyword(s):  
Crouzon Syndrome ◽  
Fgf Receptor

scholarly journals Crouzon Syndrome: a case report

2010 ◽  
Vol 3 (S1) ◽  
Author(s):  
David Reid ◽  
Stuart Morrison
Keyword(s):  
Case Report ◽  
Crouzon Syndrome

Crouzon Syndrome: Relationship of Eye Movements to Pattern Strabismus

2015 ◽  
Vol 56 (8) ◽  
pp. 4394 ◽  
Author(s):  
Avery H. Weiss ◽  
John P. Kelly ◽  
Richard A. Hopper ◽  
James O. Phillips
Keyword(s):  
Eye Movements ◽  
Crouzon Syndrome ◽  
Relationship Of

The Spheno-Occipital Synchondrosis Fuses Prematurely in Patients With Crouzon Syndrome and Midface Hypoplasia Compared With Age- and Gender-Matched Controls

2014 ◽  
Vol 72 (6) ◽  
pp. 1173-1179 ◽  
Author(s):  
Youssef Tahiri ◽  
J. Thomas Paliga ◽  
Arastoo Vossough ◽  
Scott P. Bartlett ◽  
Jesse A. Taylor
Keyword(s):  
Crouzon Syndrome ◽  
Age And Gender ◽  
Midface Hypoplasia ◽  
And Gender

A Novel FGFR2 Gene Mutation in Crouzon Syndrome Associated with Apparent Nonpenetrance

1999 ◽  
Vol 36 (6) ◽  
pp. 533-541 ◽  
Author(s):  
Eric T. Everett ◽  
Denis A. Britto ◽  
Richard E. Ward ◽  
James K. Hartsfield
Keyword(s):  
Gene Mutation ◽  
Crouzon Syndrome ◽  
Fgfr2 Gene

scholarly journals Lack of association of cranial lacunae with intracranial hypertension in children with Crouzon syndrome and Apert syndrome: a 3D morphometric quantitative analysis

2019 ◽  
Vol 35 (3) ◽  
pp. 501-507
Author(s):  
Ankita Mondal ◽  
Naiara Rodriguez-Florez ◽  
Justine O’Hara ◽  
Juling Ong ◽  
N. u. Owase Jeelani ◽  
...  
Keyword(s):  
Quantitative Analysis ◽  
Intracranial Hypertension ◽  
Apert Syndrome ◽  
Crouzon Syndrome ◽  
Hypertension In Children

Jugular Foraminal Stenosis in Crouzon Syndrome

1996 ◽  
Vol 25 (5) ◽  
pp. 252-255 ◽  
Author(s):  
Dolores Martinez-Perez ◽  
Douglas L. Vander Woude ◽  
Patrick D. Barnes ◽  
Michael Scott ◽  
John B. Mulliken
Keyword(s):  
Foraminal Stenosis ◽  
Crouzon Syndrome

scholarly journals Reducing the Burden of Care: Multidisciplinary Management of Late-Manifested Crouzon Syndrome—A Case Report

Children ◽  
2021 ◽  
Vol 8 (12) ◽  
pp. 1122
Author(s):  
Sarah Achterrath ◽  
Teresa Kruse ◽  
Julia Neuschulz ◽  
Isabelle Graf ◽  
Joachim Zöller ◽  
...  
Keyword(s):  
Quality Of Life ◽  
Case Report ◽  
Psychosocial Development ◽  
Young Patients ◽  
Crouzon Syndrome ◽  
Burden Of Care ◽  
Short Treatment ◽  
Related Quality ◽  
Health Related

The therapy of patients with Crouzon syndrome involves a multidisciplinary team. In most cases, this therapy is extensive, time-consuming, and exhausting for the patient. This case report illustrates a temporally coordinated therapy plan that succeeds in reducing the burden of care. Showing typical extraoral characteristics of Crouzon syndrome, the patient had a frontal and left-sided crossbite, and impaction of the maxillary canines. Multidisciplinary therapy included the extraction of multiple teeth, midface distraction at Le Fort III level, and alignment of the impacted teeth. Before starting, during, and after completion of the treatment, the patient’s oral health-related quality of life was assessed using COHIP-19. The combination of different treatment steps significantly reduced the duration of therapy. The therapy improved not only the patient’s oro- and craniofacial function, but also the patient’s facial appearance in a short treatment period. The patient’s quality of life improved considerably during this time. In the treatment of severe craniofacial anomalies, the highest priority should be given to keeping the burden of care low. All measures should encourage young patients’ appropriate psychosocial development despite extensive therapies, ensuring at the same time medically satisfactory treatment results.

Sign in / Sign up

Export Citation Format

Share Document