Frontonasal Dysplasia Latest Advances

A Twist1-regulated distal enhancer crucial for Alx1 gene expression and function during craniofacial development.

Journal: Developmental biology

Published: January 30, 2026

Loss of SPECC1L in cranial neural crest cells results in increased hedgehog signaling and frontonasal dysplasia.

Journal: bioRxiv : the preprint server for biology

Published: December 03, 2025

Loss of SPECC1L in cranial neural crest cells results in increased hedgehog signaling and frontonasal dysplasia.

Journal: Frontiers in physiology

Published: November 22, 2025

A novel umbrella graft approach in nasal reconstruction of patients with frontonasal dysplasia.

Journal: Journal of plastic, reconstructive & aesthetic surgery : JPRAS

Published: September 25, 2025

Cyclopia: Facial deformity indicating severe holoprosencephaly with imaging findings of brain: A case report.

Journal: Radiology case reports

Published: August 01, 2025

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

miR-302a/b/d-3p Differentially Expressed During Frontonasal Development Is Sensitive to Retinoic Acid Exposure.

Journal: Cells

Published: May 13, 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

The ALX1 transcription factor acts in the early cranial mesoderm to specify extraocular muscle formation.

Journal: Disease models & mechanisms

Published: December 04, 2024

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

Frontonasal Dysplasia Latest Advances

Find the Latest Research About Frontonasal Dysplasia

A Twist1-regulated distal enhancer crucial for Alx1 gene expression and function during craniofacial development.

A Twist1-regulated distal enhancer crucial for Alx1 gene expression and function during craniofacial development.

Loss of SPECC1L in cranial neural crest cells results in increased hedgehog signaling and frontonasal dysplasia.

Loss of SPECC1L in cranial neural crest cells results in increased hedgehog signaling and frontonasal dysplasia.

Loss of SPECC1L in cranial neural crest cells results in increased hedgehog signaling and frontonasal dysplasia.

Loss of SPECC1L in cranial neural crest cells results in increased hedgehog signaling and frontonasal dysplasia.

A novel umbrella graft approach in nasal reconstruction of patients with frontonasal dysplasia.

A novel umbrella graft approach in nasal reconstruction of patients with frontonasal dysplasia.

Cyclopia: Facial deformity indicating severe holoprosencephaly with imaging findings of brain: A case report.

Cyclopia: Facial deformity indicating severe holoprosencephaly with imaging findings of brain: A case report.

Long-Term Outcomes After Orbital Hypertelorism Correction: An Assessment of Objective Photogrammetric and Patient-Reported Outcomes.

Long-Term Outcomes After Orbital Hypertelorism Correction: An Assessment of Objective Photogrammetric and Patient-Reported Outcomes.

miR-302a/b/d-3p Differentially Expressed During Frontonasal Development Is Sensitive to Retinoic Acid Exposure.

miR-302a/b/d-3p Differentially Expressed During Frontonasal Development Is Sensitive to Retinoic Acid Exposure.

Multidisciplinary Oral Rehabilitation of Complex Frontonasal Dysplasia: A Case Report.

Multidisciplinary Oral Rehabilitation of Complex Frontonasal Dysplasia: A Case Report.

The ALX1 transcription factor acts in the early cranial mesoderm to specify extraocular muscle formation.

The ALX1 transcription factor acts in the early cranial mesoderm to specify extraocular muscle formation.

Detection of regions of homozygosity in an unusual case of frontonasal dysplasia.

Detection of regions of homozygosity in an unusual case of frontonasal dysplasia.

Genes Related to Frontonasal Malformations Are Regulated by miR-338-5p, miR-653-5p, and miR-374-5p in O9-1 Cells.

Genes Related to Frontonasal Malformations Are Regulated by miR-338-5p, miR-653-5p, and miR-374-5p in O9-1 Cells.

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.

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.