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Saethre-Chotzen Syndrome: A Report of 7 Patients and Review of the Literature.
Abulezz TA, Allam KA, Wan DC, Lee JC, Kawamoto HK. Abulezz TA, et al. Ann Plast Surg. 2020 Sep;85(3):251-255. doi: 10.1097/SAP.0000000000002391. Ann Plast Surg. 2020. PMID: 32487807 Review.
INTRODUCTION: Saethre-Chotzen syndrome is a genetic condition characterized by craniofacial and limb anomalies, with craniosynostosis (mainly coronal) being the most frequent craniofacial finding. ...METHODS: A retrospective review was performed on records of …
INTRODUCTION: Saethre-Chotzen syndrome is a genetic condition characterized by craniofacial and limb anomalies, with cr …
Saethre-Chotzen syndrome: Case report and literature review.
Pelc A, Mikulewicz M. Pelc A, et al. Dent Med Probl. 2018 Apr-Jun;55(2):217-225. doi: 10.17219/dmp/91050. Dent Med Probl. 2018. PMID: 30152628 Free article. Review.
Saethre-Chotzen syndrome (SCS) belongs to a group of rare congenital disorders connected with craniosynostosis and syndactyly. ...
Saethre-Chotzen syndrome (SCS) belongs to a group of rare congenital disorders connected with craniosynostosis and synd …
Saethre-Chotzen syndrome: long-term outcome of a syndrome-specific management protocol.
Den Ottelander BK, Van Veelen MC, De Goederen R, Van De Beeten SD, Dremmen MH, Loudon SE, Versnel SL, Van Den Ouweland AM, Van Dooren MF, Joosten KF, Mathijssen IM. Den Ottelander BK, et al. Dev Med Child Neurol. 2021 Jan;63(1):104-110. doi: 10.1111/dmcn.14670. Epub 2020 Sep 9. Dev Med Child Neurol. 2021. PMID: 32909287 Free PMC article.
AIM: To assess the long-term outcomes of our management protocol for Saethre-Chotzen syndrome, which includes one-stage fronto-orbital advancement. METHOD: All patients born with Saethre-Chotzen syndrome between January 1992 and March 201 …
AIM: To assess the long-term outcomes of our management protocol for Saethre-Chotzen syndrome, which includes one-stage …
Craniofacial morphology and growth in Muenke syndrome, Saethre-Chotzen syndrome, and TCF12-related craniosynostosis.
Choi TM, Lijten OW, Mathijssen IMJ, Wolvius EB, Ongkosuwito EM. Choi TM, et al. Clin Oral Investig. 2022 Mar;26(3):2927-2936. doi: 10.1007/s00784-021-04275-y. Epub 2021 Dec 14. Clin Oral Investig. 2022. PMID: 34904178 Free PMC article.
CONCLUSIONS: In this study, we showed that the midface is hypoplastic in Muenke syndrome, Saethre-Chotzen syndrome, and TCF12-related craniosynostosis compared to the Dutch control group. ...CLINICAL RELEVANCE: The maxillary growth in patients with Muenke syn …
CONCLUSIONS: In this study, we showed that the midface is hypoplastic in Muenke syndrome, Saethre-Chotzen syndrome, and …
Evaluation of dental maturity in Muenke syndrome, Saethre-Chotzen syndrome, and TCF12-related craniosynostosis.
Choi TM, Kramer GJC, Goos JAC, Mathijssen IMJ, Wolvius EB, Ongkosuwito EM. Choi TM, et al. Eur J Orthod. 2022 May 24;44(3):287-293. doi: 10.1093/ejo/cjab056. Eur J Orthod. 2022. PMID: 34424951 Free PMC article.
OBJECTIVES: To determine whether dental maturity (dental development) was delayed in patients with Muenke syndrome, Saethre-Chotzen syndrome, and TCF12-related craniosynostosis, compared with a Dutch control group without syndromes. ...CONCLUSIONS: Our result …
OBJECTIVES: To determine whether dental maturity (dental development) was delayed in patients with Muenke syndrome, Saethre-Chotze …
Lateral and Frontal Cephalometric Measurements in a Cohort With Saethre-Chotzen Syndrome.
Rizell S, Karlsson P, Ransjö M, Westerlund A, Yehia Z, Kölby L. Rizell S, et al. Cleft Palate Craniofac J. 2021 Jul;58(7):838-846. doi: 10.1177/1055665620969292. Epub 2020 Nov 6. Cleft Palate Craniofac J. 2021. PMID: 33153317
OBJECTIVE: Descriptions of the craniofacial morphology in Saethre-Chotzen syndrome (SCS) are primarily based on case reports or visual assessments of affected families. ...METHODS: Cephalometric measurements were performed using lateral and frontal cephalogra …
OBJECTIVE: Descriptions of the craniofacial morphology in Saethre-Chotzen syndrome (SCS) are primarily based on case re …
Progressive Postnatal Pansynostosis.
Rogers GF, Greene AK, Proctor MR, Mulliken JB, Goobie SM, Stoler JM. Rogers GF, et al. Cleft Palate Craniofac J. 2015 Nov;52(6):751-7. doi: 10.1597/14-092. Epub 2014 Oct 28. Cleft Palate Craniofac J. 2015. PMID: 25350344
Fifteen patients had a syndromic diagnosis: Crouzon syndrome (n = 8), Saethre-Chotzen syndrome (n = 5), and Pfeiffer syndrome (n = 2). With the exception of one patient with moderate turricephaly, all patients had a relatively normal head shape with cranial i …
Fifteen patients had a syndromic diagnosis: Crouzon syndrome (n = 8), Saethre-Chotzen syndrome (n = 5), and Pfeiffer sy …
Saethre-Chotzen syndrome: a clinical, EEG and neuroradiological study.
Elia M, Musumeci SA, Ferri R, Greco D, Romano C, Del Gracco S, Stefanini MC. Elia M, et al. Childs Nerv Syst. 1996 Nov;12(11):699-704. doi: 10.1007/BF00366154. Childs Nerv Syst. 1996. PMID: 9118134
Saethre-Chotzen syndrome is a form of acrocephalosyndactyly with autosomal dominant inheritance, characterized by craniosynostosis, facial asymmetry, palpebral ptosis, deviated nasal septum, partial cutaneous syndactyly, and various skeletal abnormalities. .. …
Saethre-Chotzen syndrome is a form of acrocephalosyndactyly with autosomal dominant inheritance, characterized by crani …
Reoperation for intracranial hypertension in TWIST1-confirmed Saethre-Chotzen syndrome: a 15-year review.
Woods RH, Ul-Haq E, Wilkie AOM, Jayamohan J, Richards PG, Johnson D, Lester T, Wall SA. Woods RH, et al. Plast Reconstr Surg. 2009 Jun;123(6):1801-1810. doi: 10.1097/PRS.0b013e3181a3f391. Plast Reconstr Surg. 2009. PMID: 19483581 Free PMC article. Review.
BACKGROUND: Saethre-Chotzen syndrome is a syndromic craniosynostosis defined by a genetic mutation affecting the TWIST1 gene on chromosome 7p21. ...CONCLUSIONS: Despite standard surgical intervention, patients with Saethre-Chotzen syndrome …
BACKGROUND: Saethre-Chotzen syndrome is a syndromic craniosynostosis defined by a genetic mutation affecting the TWIST1 …
Audiologic findings in Saethre-Chotzen syndrome.
Rosen H, Andrews BT, Meara JG, Stoler JM, Mulliken JB, Rogers GF. Rosen H, et al. Plast Reconstr Surg. 2011 May;127(5):2014-2020. doi: 10.1097/PRS.0b013e31820cf16a. Plast Reconstr Surg. 2011. PMID: 21532428
METHODS: The authors retrospectively reviewed the audiologic and otologic records of patients with Saethre-Chotzen syndrome to define the incidence, type, and extent of hearing loss. ...Twenty-one patients (72 percent) had normal hearing on their last audiogr …
METHODS: The authors retrospectively reviewed the audiologic and otologic records of patients with Saethre-Chotzen syndrome …
65 results