Acrocephalopolydactyly Latest Advances

Find the Latest Research About Acrocephalopolydactyly

Last Updated: 09/26/2026

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Found 1943 publications

Congenital structural respiratory disorders as the root cause of pediatric obstructive sleep apnea syndrome in Apert syndrome

Congenital structural respiratory disorders as the root cause of pediatric obstructive sleep apnea syndrome in Apert syndrome

Journal: Zhurnal nevrologii i psikhiatrii imeni S.S. Korsakova
Published: September 01, 2026

Patient-Specific 3D Printed Palatal Protection Plates for Le Fort III Osteotomy in Syndromic Midface Hypoplasia: What We Do.

Patient-Specific 3D Printed Palatal Protection Plates for Le Fort III Osteotomy in Syndromic Midface Hypoplasia: What We Do.

Journal: The Cleft palate-craniofacial journal : official publication of the American Cleft Palate-Craniofacial Association
Published: July 01, 2026

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

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

Journal: Plastic and reconstructive surgery
Published: June 24, 2026

Sphenopalatine Artery Pseudoaneurysm as a Rare Complication of Le Fort III Advancement in Apert Syndrome.

Sphenopalatine Artery Pseudoaneurysm as a Rare Complication of Le Fort III Advancement in Apert Syndrome.

Journal: The Journal of craniofacial surgery
Published: May 24, 2026

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.

Journal: AJNR. American journal of neuroradiology
Published: May 23, 2026

Apert Syndrome: Oral, Maxillofacial and Dental Management-A Narrative Clinical Review.

Apert Syndrome: Oral, Maxillofacial and Dental Management-A Narrative Clinical Review.

Journal: Clinics and practice
Published: May 06, 2026

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.

Journal: Turkish archives of pediatrics
Published: May 05, 2026

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

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

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.

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.

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.

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
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Last Updated: 09/26/2026