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About 123 results

ALLMedicine™ Saethre-Chotzen Syndrome Center

Research & Reviews  49 results

Postnatal Progressive Craniosynostosis in Syndromic Conditions: Two Patients With Saeth...
https://doi.org/10.1177/10556656221090844
The Cleft Palate-craniofacial Journal : Official Publicat... Alawneh RJ, Johnson AL et. al.

Apr 1st, 2022 - Saethre-Chotzen syndrome (SCS) is a known craniosynostosis syndrome with a variable presentation of craniofacial and somatic involvement. Congenital coronal craniosynostosis is most commonly observed in SCS; however, progressive postnatal craniosy...

Quantitative Morphologic Analysis of Cranial Vault in Twist1+/- Mice: Implications in C...
https://doi.org/10.1097/PRS.0000000000008665
Plastic and Reconstructive Surgery; Nuri T, Ota M et. al.

Dec 23rd, 2021 - The haploinsufficiency in the TWIST1 gene encoding a basic helix-loop-helix transcription factor is a cause of one of the craniosynostosis syndromes, Saethre-Chotzen syndrome. Patients with craniosynostosis usually require operative release of aff...

Craniofacial morphology and growth in Muenke syndrome, Saethre-Chotzen syndrome, and TC...
https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8898243
Clinical Oral Investigations; Choi TM, Lijten OW et. al.

Dec 15th, 2021 - To determine whether the midface of patients with Muenke syndrome, Saethre-Chotzen syndrome, or TCF12-related craniosynostosis is hypoplastic compared to skeletal facial proportions of a Dutch control group. We included seventy-four patients (43 p...

Facial Dysmorphology in Saethre-Chotzen Syndrome.
https://doi.org/10.1097/SCS.0000000000007910
The Journal of Craniofacial Surgery; Junn A, Dinis J et. al.

Nov 3rd, 2021 - Classic features of Saethre-Chotzen syndrome (SCS) described in the literature include a prominent nasal bridge, eyelid ptosis, telorbitism, maxillary hypoplasia, and mandibular prognathism. The purpose of this study was to evaluate objectively th...

Syndrome-related outcomes following posterior vault distraction osteogenesis.
https://doi.org/10.1007/s00381-021-05169-w 10.1097/PRS.0b013e31820a64b6 10.1097/SCS.0000000000004353 10.1097/SCS.0b013e318240ff49 10.1097/SCS.0000000000005285 10.1097/SLA.0b013e3181b13ca2 10.1007/s00381-012-1802-0 10.1097/PRS.0000000000001294 10.2119/2007-00027.Fanganiello 10.1097/PRS.0b013e3182729f42 10.1016/j.jcms.2014.11.023 10.1097/PRS.0b013e31828bd541 10.1097/PRS.0000000000006041 10.1097/PRS.0b013e31818458f0 10.1097/SCS.0000000000005496 10.1097/SCS.0000000000003458 10.1007/s00381-019-04059-6 10.1007/s00381-011-1563-1 10.1055/s-0034-1390169 10.1097/SCS.0000000000004098 10.1097/GOX.0000000000002230 10.1097/PRS.0000000000004815 10.1097/GOX.0000000000002788 10.1097/SCS.0000000000006105 10.1097/PRS.0000000000006646 10.3171/jns.1982.57.3.0370 10.1097/SCS.0000000000002661 10.1007/s00381-010-1353-1 10.1097/SCS.0000000000002739 10.1097/PRS.0b013e318200ab83 10.1097/PRS.0000000000002127 10.1007/s00381-019-04448-x 10.1097/SCS.0000000000004473 10.1007/BF00301758 10.1007/s00381-008-0758-6 10.1097/SCS.0b013e31819b9429 10.1016/j.jcms.2012.02.018 10.1097/PRS.0b013e3181a3f391
Child's Nervous System : ChNS : Official Journal of the I... Raposo-Amaral CE, de Oliveira YM et. al.

Apr 19th, 2021 - The most commonly occurring syndromic craniosynostoses are Apert syndrome, Crouzon syndrome, Pfeiffer syndrome, and Saethre-Chotzen syndrome. There is insufficient data regarding postoperative syndrome-related outcomes following the posterior vaul...

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