Skip to main page content
U.S. flag

An official website of the United States government

Dot gov

The .gov means it’s official.
Federal government websites often end in .gov or .mil. Before sharing sensitive information, make sure you’re on a federal government site.

Https

The site is secure.
The https:// ensures that you are connecting to the official website and that any information you provide is encrypted and transmitted securely.

Access keys NCBI Homepage MyNCBI Homepage Main Content Main Navigation

Search Page

Filters

My NCBI Filters

Results by year

Table representation of search results timeline featuring number of search results per year.

Year Number of Results
2003 1
2007 2
2008 1
2009 1
2010 2
2011 4
2013 2
2014 2
2015 3
2017 1
2018 3
2019 1
2020 3
2021 5
2024 0

Text availability

Article attribute

Article type

Publication date

Search Results

27 results

Results by year

Filters applied: . Clear all
Page 1
Glaucoma With Crouzon Syndrome.
Alshamrani AA, Al-Shahwan S. Alshamrani AA, et al. J Glaucoma. 2018 Jun;27(6):e110-e112. doi: 10.1097/IJG.0000000000000946. J Glaucoma. 2018. PMID: 29557836
BACKGROUND: Crouzon syndrome is the most common form of craniosynostosis, and mutations in the fibroblast growth factor receptor 2 and 3 (FGFR2 and FGFR3) genes are implicated in its pathogenesis. OBSERVATION: A 10-year-old female patient with Crouzon synd …
BACKGROUND: Crouzon syndrome is the most common form of craniosynostosis, and mutations in the fibroblast growth factor recept …
Syndrome-related outcomes following posterior vault distraction osteogenesis.
Raposo-Amaral CE, de Oliveira YM, Denadai R, Raposo-Amaral CA, Ghizoni E. Raposo-Amaral CE, et al. Childs Nerv Syst. 2021 Jun;37(6):2001-2009. doi: 10.1007/s00381-021-05169-w. Epub 2021 Apr 18. Childs Nerv Syst. 2021. PMID: 33866411
PURPOSE: The most commonly occurring syndromic craniosynostoses are Apert syndrome, Crouzon syndrome, Pfeiffer syndrome, and Saethre-Chotzen syndrome. ...Apert syndrome patients presented relatively higher total blood transfusion rates than Crouzon syndrom …
PURPOSE: The most commonly occurring syndromic craniosynostoses are Apert syndrome, Crouzon syndrome, Pfeiffer syndrome, and S …
Severe chemosis and treatment following fronto-orbital advancement surgery for Crouzon syndrome: A case report.
Wu SH, Liu TJ, Fan SS, Chen ZH, Wang XL, Gu S. Wu SH, et al. Medicine (Baltimore). 2021 Feb 19;100(7):e24693. doi: 10.1097/MD.0000000000024693. Medicine (Baltimore). 2021. PMID: 33607809 Free PMC article.
RATIONALE: Crouzon syndrome is a craniofacial malformation caused by premature fusion of fibrous sutures in infants. ...Our report describes 2 rare complications associated with the treatment for Crouzon syndrome, and we believe it will be of use to cl …
RATIONALE: Crouzon syndrome is a craniofacial malformation caused by premature fusion of fibrous sutures in infants. ...Our re …
Cervical Spinal Cord Compression and Sleep-Disordered Breathing in Syndromic Craniosynostosis.
den Ottelander BK, de Goederen R, de Planque CA, Baart SJ, van Veelen MLC, Corel LJA, Joosten KFM, Mathijssen IMJ, Dremmen MHG. den Ottelander BK, et al. AJNR Am J Neuroradiol. 2021 Jan;42(1):201-205. doi: 10.3174/ajnr.A6881. Epub 2020 Dec 3. AJNR Am J Neuroradiol. 2021. PMID: 33272949 Free PMC article.

The compression ratio at the level of the odontoid process was comparable with that in controls; the compression ratio at the level of the foramen magnum was significantly higher in patients with Crouzon syndrome (+27.1, P < .001). The cervicomedullary angle was

…
The compression ratio at the level of the odontoid process was comparable with that in controls; the compression ratio at the level of the f …
Distraction osteogenesis in the surgical management of syndromic craniosynostosis: a comprehensive review of published papers.
Al-Namnam NMN, Hariri F, Rahman ZAA. Al-Namnam NMN, et al. Br J Oral Maxillofac Surg. 2018 Jun;56(5):353-366. doi: 10.1016/j.bjoms.2018.03.002. Epub 2018 Apr 13. Br J Oral Maxillofac Surg. 2018. PMID: 29661509 Review.
The search was confined to publications in English, and we followed the guidelines of the PRISMA statement. We found that deformity of the skull resulted mainly from Crouzon syndrome. Recently craniofacial distraction has been achieved by monobloc distraction osteog …
The search was confined to publications in English, and we followed the guidelines of the PRISMA statement. We found that deformity of the s …
Prevalence of selected congenital anomalies in Saudi children: a community-based study.
AlSalloum A, El Mouzan MI, AlHerbish A, AlOmer A, Qurashi M. AlSalloum A, et al. Ann Saudi Med. 2015 Mar-Apr;35(2):107-10. doi: 10.5144/0256-4947.2015.107. Ann Saudi Med. 2015. PMID: 26336015 Free PMC article.
SUBJECTS AND METHODS: The study sample was determined by a multi-stage probability random sampling of household representatives of the Saudi Arab population. ...The prevalence of cleft lip with or without cleft palate was 0.9 per 10000 children, achondroplasia was 0.7 per …
SUBJECTS AND METHODS: The study sample was determined by a multi-stage probability random sampling of household representatives of th …
Surgical Outcome After Less "Rigid" Fixation in Open Cranial Vault Remodeling for Craniosynostosis.
Koh KL, Zain A. Koh KL, et al. J Craniofac Surg. 2018 Jun;29(4):861-867. doi: 10.1097/SCS.0000000000004347. J Craniofac Surg. 2018. PMID: 29438206
Sixteen patients were syndromic with multiple suture synostoses: Apert syndrome (n = 8), Crouzon syndrome (n = 6), and Muenke's syndrome (n = 2). Eighteen patients were nonsyndromic: isolated single-suture craniosynostosis (n = 12) and multiple suture involvement (n …
Sixteen patients were syndromic with multiple suture synostoses: Apert syndrome (n = 8), Crouzon syndrome (n = 6), and Muenke' …
High Le Fort I and bilateral split sagittal osteotomy in Crouzon syndrome.
Tay YC, Tan KH, Yeow VK. Tay YC, et al. J Craniofac Surg. 2013 May;24(3):e253-5. doi: 10.1097/SCS.0b013e3182869f40. J Craniofac Surg. 2013. PMID: 23714981
Crouzon syndrome is a rare, autosomal dominant disease from a fibroblast growth factor receptor 2 gene mutation, characterized by premature craniosynostosis, hypertelorism, orbital proptosis, psittichorina, hypoplastic maxilla, and mandibular prognathism. We present …
Crouzon syndrome is a rare, autosomal dominant disease from a fibroblast growth factor receptor 2 gene mutation, characterized …
Complications in 54 frontofacial distraction procedures in patients with syndromic craniosynostosis.
Goldstein JA, Paliga JT, Taylor JA, Bartlett SP. Goldstein JA, et al. J Craniofac Surg. 2015 Jan;26(1):124-8. doi: 10.1097/SCS.0000000000001320. J Craniofac Surg. 2015. PMID: 25569391
Chi-squared and Fisher exact test were used to compare variables.From 1999 to 2012, a total of 54 patients underwent midface distraction osteogenesis, including 23 patients with Apert syndrome, 19 patients with Crouzon syndrome, 10 patients with Pfeiffer syndrome, a …
Chi-squared and Fisher exact test were used to compare variables.From 1999 to 2012, a total of 54 patients underwent midface distraction ost …
27 results