Saethre-Chotzen Syndrome Latest Advances

Hypoplastic vestibular aqueduct in congenital temporal bone anomalies - implications for subtype diagnosis of Meniere's disease.

Journal: AJNR. American journal of neuroradiology

Published: May 23, 2026

The Clinical and Molecular Spectrum of Turkish Patients with Syndromic Craniosynostosis: A Single Center Study.

Journal: Turkish archives of pediatrics

Published: May 05, 2026

Spring-Assisted Cranioplasty in Multisuture Craniosynostosis: Initial Experience From Thailand.

Journal: The Journal of craniofacial surgery

Published: April 30, 2026

Ocular manifestations of Apert syndrome: a case report

Journal: [Zhonghua yan ke za zhi] Chinese journal of ophthalmology

Published: April 07, 2026

Bilateral Posterior Ischemic Optic Neuropathy Following Midface Advancement Surgery in a Pediatric Patient With Pfeiffer Syndrome.

Journal: The Journal of craniofacial surgery

Published: March 19, 2026

Navigating challenges: a child with Apert syndrome and global developmental delay from a low-income family.

Journal: BMJ case reports

Published: March 05, 2026

Long-term survival without high cancer risk in a cohort of 24 patients with Apert syndrome.

Journal: European journal of human genetics : EJHG

Published: February 18, 2026

Towards consensus on the treatment of congenital craniofacial conditions: the discussion section of a doctoral thesis.

Journal: Journal of plastic surgery and hand surgery

Published: February 16, 2026

Early Motor Development and Rehabilitation Outcomes in Apert Syndrome: Gross Motor Function Measures-Case Report.

Journal: Pathophysiology : the official journal of the International Society for Pathophysiology

Published: January 16, 2026

Bilateral coronal craniosynostosis with novel TWIST1 mutation.

Journal: Child's nervous system : ChNS : official journal of the International Society for Pediatric Neurosurgery

Published: January 15, 2026

The Impact of Genetics on Craniofacial Dysplasias and Consequent Oral Malformations-Integrative Review.

Journal: Genes

Published: December 17, 2025

The APERT Severity Scale: A Quantitative Tool for Risk Stratification in Apert Syndrome.

Journal: Plastic and reconstructive surgery

Published: December 16, 2025

Saethre-Chotzen Syndrome Latest Advances

Find the Latest Research About Saethre-Chotzen Syndrome

Hypoplastic vestibular aqueduct in congenital temporal bone anomalies - implications for subtype diagnosis of Meniere's disease.

Hypoplastic vestibular aqueduct in congenital temporal bone anomalies - implications for subtype diagnosis of Meniere's disease.

The Clinical and Molecular Spectrum of Turkish Patients with Syndromic Craniosynostosis: A Single Center Study.

The Clinical and Molecular Spectrum of Turkish Patients with Syndromic Craniosynostosis: A Single Center Study.

Spring-Assisted Cranioplasty in Multisuture Craniosynostosis: Initial Experience From Thailand.

Spring-Assisted Cranioplasty in Multisuture Craniosynostosis: Initial Experience From Thailand.

Ocular manifestations of Apert syndrome: a case report

Ocular manifestations of Apert syndrome: a case report

Bilateral Posterior Ischemic Optic Neuropathy Following Midface Advancement Surgery in a Pediatric Patient With Pfeiffer Syndrome.

Bilateral Posterior Ischemic Optic Neuropathy Following Midface Advancement Surgery in a Pediatric Patient With Pfeiffer Syndrome.

Navigating challenges: a child with Apert syndrome and global developmental delay from a low-income family.

Navigating challenges: a child with Apert syndrome and global developmental delay from a low-income family.

Long-term survival without high cancer risk in a cohort of 24 patients with Apert syndrome.

Long-term survival without high cancer risk in a cohort of 24 patients with Apert syndrome.

Towards consensus on the treatment of congenital craniofacial conditions: the discussion section of a doctoral thesis.

Towards consensus on the treatment of congenital craniofacial conditions: the discussion section of a doctoral thesis.

Early Motor Development and Rehabilitation Outcomes in Apert Syndrome: Gross Motor Function Measures-Case Report.

Early Motor Development and Rehabilitation Outcomes in Apert Syndrome: Gross Motor Function Measures-Case Report.

Bilateral coronal craniosynostosis with novel TWIST1 mutation.

Bilateral coronal craniosynostosis with novel TWIST1 mutation.

The Impact of Genetics on Craniofacial Dysplasias and Consequent Oral Malformations-Integrative Review.

The Impact of Genetics on Craniofacial Dysplasias and Consequent Oral Malformations-Integrative Review.

The APERT Severity Scale: A Quantitative Tool for Risk Stratification in Apert Syndrome.

The APERT Severity Scale: A Quantitative Tool for Risk Stratification in Apert Syndrome.