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1983 1
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2023 2
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Page 1
Velopharyngeal Insufficiency in Craniofacial Microsomia: Prevalence, Diagnosis, and Treatment.
Chan CH, Hu AC, Jain NS, Dang BN, Liu MT, Bertrand AA, Wilson LF, Lee JC. Chan CH, et al. J Craniofac Surg. 2021 Nov-Dec 01;32(8):2771-2773. doi: 10.1097/SCS.0000000000007938. J Craniofac Surg. 2021. PMID: 34727477
Of the patients with isolated CFM and VPI, 8 patients (66.7%) were recommended for nasoendoscopy, of which only 2 patients completed. Seven isolated CFM patients (58.3%) underwent speech therapy, whereas none received VPI surgery. ...In addition, despite clinical di …
Of the patients with isolated CFM and VPI, 8 patients (66.7%) were recommended for nasoendoscopy, of which only 2 patients completed. Seven …
Novel risk factors for craniofacial microsomia and assessment of their utility in clinic diagnosis.
Xu X, Wang B, Jiang Z, Chen Q, Mao K, Shi X, Yan C, Hu J, Zha Y, Ma C, Zhang J, Guo R, Wang L, Zhao S, Liu H, Zhang Q, Zhang YB. Xu X, et al. Hum Mol Genet. 2021 May 31;30(11):1045-1056. doi: 10.1093/hmg/ddab055. Hum Mol Genet. 2021. PMID: 33615373
Single-nucleotide polymorphism-based PRS is significantly associated with CFM [P = 7.22 10-58, odds ratio = 3.15, 95% confidence interval (CI) 2.74-3.63], and the top fifth percentile has a 6.8-fold CFM risk comparing with the 10th percentile. ...
Single-nucleotide polymorphism-based PRS is significantly associated with CFM [P = 7.22 10-58, odds ratio = 3.15, 95% confidence inte …
Psychosocial and Health-Related Experiences of Individuals With Microtia and Craniofacial Microsomia and Their Families: Narrative Review Over 2 Decades.
Johns AL, Stock NM, Costa B, Billaud Feragen K, Crerand CE. Johns AL, et al. Cleft Palate Craniofac J. 2023 Sep;60(9):1090-1112. doi: 10.1177/10556656221091699. Epub 2022 Apr 5. Cleft Palate Craniofac J. 2023. PMID: 35382590 Free PMC article. Review.
Studies addressed 5 primary topics: (1) Healthcare Experiences, including Medical Care, Hearing Loss/Amplification, Diagnostic Experiences, and Information Preferences; (2) Psychosocial Experiences, including Teasing, Behavioral Adjustment, Psychosocial Support, and Public …
Studies addressed 5 primary topics: (1) Healthcare Experiences, including Medical Care, Hearing Loss/Amplification, Diagnostic Experi …
Evaluating International Diagnostic, Screening, and Monitoring Practices for Craniofacial Microsomia and Microtia: A Survey Study.
Ronde EM, Nolte JW, Kruisinga FH, Maas SM, Lapid O, Ebbens FA, Becking AG, Breugem CC. Ronde EM, et al. Cleft Palate Craniofac J. 2023 Sep;60(9):1118-1127. doi: 10.1177/10556656221093912. Epub 2022 Apr 26. Cleft Palate Craniofac J. 2023. PMID: 35469463 Free PMC article.
Fifty-seven responses were received from 30 countries (response rate 3%).The International Consortium for Health Outcomes Measurement diagnostic criteria were used by 86% of respondents, though 65% considered isolated microtia a mild form of CFM. ...Respondents mostly supp …
Fifty-seven responses were received from 30 countries (response rate 3%).The International Consortium for Health Outcomes Measurement …
Treacher Collins syndrome: protocol management from birth to maturity.
Thompson JT, Anderson PJ, David DJ. Thompson JT, et al. J Craniofac Surg. 2009 Nov;20(6):2028-35. doi: 10.1097/SCS.0b013e3181be8788. J Craniofac Surg. 2009. PMID: 19881372
BACKGROUND: : Management of patients with Treacher Collins syndrome is complicated and involves multiple disciplines working in concert to achieve a common outcome. ...The records of these patients were reviewed to establish what interventions they required a …
BACKGROUND: : Management of patients with Treacher Collins syndrome is complicated and involves multiple disciplines wo …
Treatment modalities of infants with upper airway obstruction--review of the literature and presentation of novel orthopedic appliances.
Kochel J, Meyer-Marcotty P, Wirbelauer J, Böhm H, Kochel M, Thomas W, Bareis U, Hebestreit H, Speer C, Stellzig-Eisenhauer A. Kochel J, et al. Cleft Palate Craniofac J. 2011 Jan;48(1):44-55. doi: 10.1597/08-273. Epub 2010 Apr 7. Cleft Palate Craniofac J. 2011. PMID: 20500074 Review.
Patients with type 1 obstruction received a plate with an epiglottic spur; whereas, patients with obstruction type 2, 3, or 4 received a plate with a pharyngeal tube. RESULTS: All patients were successfully treated with orthopedic appliances alone. Under plate therapy
Patients with type 1 obstruction received a plate with an epiglottic spur; whereas, patients with obstruction type 2, 3, or 4 receive …
Prenatal Diagnosis of Fetal Micrognathia at 11-20 Weeks of Gestation: A Prospective Observation Study.
Wu S, Han J, Duan G, Xue J, Huang R, Wu L, Yan X, Pi H, Yang X. Wu S, et al. J Ultrasound Med. 2024 Mar;43(3):491-499. doi: 10.1002/jum.16379. Epub 2024 Jan 2. J Ultrasound Med. 2024. PMID: 38164991
A total of 78.9% (15/19) cases had a genetic cause confirmed, including 12 with chromosomal abnormalities and 3 with monogenic disorders. Monogenic disorders were all known causes of micrognathia, including two cases of campomelic dysplasia affected by SOX9 mutations and o …
A total of 78.9% (15/19) cases had a genetic cause confirmed, including 12 with chromosomal abnormalities and 3 with monogenic disord …
Prenatal diagnosis of Nager syndrome in a 12-week-old fetus with a whole gene deletion of SF3B4 by chromosomal microarray.
Lund IC, Vestergaard EM, Christensen R, Uldbjerg N, Becher N. Lund IC, et al. Eur J Med Genet. 2016 Jan;59(1):48-51. doi: 10.1016/j.ejmg.2015.12.001. Epub 2015 Dec 9. Eur J Med Genet. 2016. PMID: 26679067
Less than one hundred cases of the acrofacial dysostosis, Nager syndrome, have been described. The cardinal features of Nager syndrome are micrognathia, midface retrusion and limb malformations, predominately of the radial ray of upper extremities. Within the …
Less than one hundred cases of the acrofacial dysostosis, Nager syndrome, have been described. The cardinal features of Nager …
Craniofacial Microsomia: Orthodontic Surgical Treatment of Growing Patients.
Agurto Veas P, Castellón Zirpel L, Morovic CG. Agurto Veas P, et al. J Craniofac Surg. 2018 Sep;29(6):1426-1429. doi: 10.1097/SCS.0000000000004821. J Craniofac Surg. 2018. PMID: 30015747
Due to the vast phenotypic variation and complexity of the malformation, a global treatment that is coordinated by a multidisciplinary team is imperative. Herein, the authors describe 3 clinical patients and discuss the different therapies used according to the type …
Due to the vast phenotypic variation and complexity of the malformation, a global treatment that is coordinated by a multidisciplinary team …
Exploring the Medical and Psychosocial Concerns of Adolescents and Young Adults With Craniofacial Microsomia: A Qualitative Study.
Hamilton KV, Ormond KE, Moscarello T, Bruce JS, Bereknyei Merrell S, Chang KW, Bernstein JA. Hamilton KV, et al. Cleft Palate Craniofac J. 2018 Nov;55(10):1430-1439. doi: 10.1177/1055665618768542. Epub 2018 Apr 10. Cleft Palate Craniofac J. 2018. PMID: 29634364
RESULTS: Five themes were evident in the data: (1) impact on personal growth and character development, (2) negative psychosocial impact, (3) deciding to hide or reveal the condition, (4) desire to make personal surgical decisions, and (5) struggles with hearing loss. ...
RESULTS: Five themes were evident in the data: (1) impact on personal growth and character development, (2) negative psychosocial impact, ( …
17 results