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Last Updated: 10/31/2025
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Found 235 publications
Long-Term Outcomes After Orbital Hypertelorism Correction: An Assessment of Objective Photogrammetric and Patient-Reported Outcomes.
Journal: The Journal of craniofacial surgery
Published: July 16, 2025
Multidisciplinary Oral Rehabilitation of Complex Frontonasal Dysplasia: A Case Report.
Journal: The Cleft palate-craniofacial journal : official publication of the American Cleft Palate-Craniofacial Association
Published: January 09, 2025
Detection of regions of homozygosity in an unusual case of frontonasal dysplasia.
Journal: Molecular cytogenetics
Published: June 17, 2024
Genes Related to Frontonasal Malformations Are Regulated by miR-338-5p, miR-653-5p, and miR-374-5p in O9-1 Cells.
Journal: Journal of developmental biology
Published: April 02, 2024
Prenatal diagnosis of a severe form of frontonasal dysplasia with severe limb anomalies, hydrocephaly, a hypoplastic corpus callosum, and a ventricular septal defect using 3D ultrasound: a case report and literature review.
Journal: BMC pregnancy and childbirth
Published: February 18, 2024
A rare homozygous ALX4 mutation in a Bangladeshi girl with frontonasal dysplasia type-2 (FND2).
Journal: Heliyon
Published: January 15, 2024
Lineage-specific requirements of Alx4 function in craniofacial and hair development.
Journal: Developmental dynamics : an official publication of the American Association of Anatomists
Published: January 10, 2024
Designing custom three-dimensional printed eyeglasses for children with frontonasal abnormalities: addressing challenges in access and fit.
Journal: Journal of AAPOS : the official publication of the American Association for Pediatric Ophthalmology and Strabismus
Published: December 02, 2023
Structural Rhinoplasty as an Effective Surgical Approach for Frontonasal Dysplasia.
Journal: The Journal of craniofacial surgery
Published: November 16, 2023
Frontonasal Dysplasia: A Clinical Dilemma.
Journal: Journal of maxillofacial and oral surgery
Published: August 07, 2023
BTB domain mutations perturbing KCTD15 oligomerisation cause a distinctive frontonasal dysplasia syndrome.
Journal: Journal of medical genetics
Published: July 24, 2023
Last Updated: 10/31/2025