Lacrimo-Auriculo-Dento-Digital Syndrome Latest Advances

Find the Latest Research About Lacrimo-Auriculo-Dento-Digital Syndrome

Last Updated: 04/28/2026

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Found 76 publications

Complete congenital agenesis of major salivary glands: case report and systematic review of the literature.

Complete congenital agenesis of major salivary glands: case report and systematic review of the literature.

Journal: Journal of stomatology, oral and maxillofacial surgery
Published: December 24, 2025

Esophageal Atresia, an Anomaly of VACTERL Association or Novel Feature of the FGF10 Gene: A Case Report.

Esophageal Atresia, an Anomaly of VACTERL Association or Novel Feature of the FGF10 Gene: A Case Report.

Journal: Molecular syndromology
Published: March 24, 2025

CATSHL syndrome, a new family and phenotypic expansion.

CATSHL syndrome, a new family and phenotypic expansion.

Journal: Clinical genetics
Published: September 14, 2023

Bilateral Nasolacrimal Duct Obstruction Managed With Probing and Irrigation in a Patient With FGF10-Associated Lacrimo-auriculo-dento-digital Syndrome.

Bilateral Nasolacrimal Duct Obstruction Managed With Probing and Irrigation in a Patient With FGF10-Associated Lacrimo-auriculo-dento-digital Syndrome.

Journal: Journal of pediatric ophthalmology and strabismus
Published: July 21, 2023

Variants in FGF10 cause early onset of severe childhood interstitial lung disease: A detailed description of four affected children.

Variants in FGF10 cause early onset of severe childhood interstitial lung disease: A detailed description of four affected children.

Journal: Pediatric pulmonology
Published: May 22, 2023

Craniofacial anomalies in a murine model of heterozygous fibroblast growth factor 10 gene mutation.

Craniofacial anomalies in a murine model of heterozygous fibroblast growth factor 10 gene mutation.

Journal: Orthodontics & craniofacial research
Published: February 06, 2023

Identification of a novel mutation in the FGF10 gene in a Chinese family with obvious congenital lacrimal duct dysplasia in lacrimo-auriculo-dento-digital syndrome.

Identification of a novel mutation in the FGF10 gene in a Chinese family with obvious congenital lacrimal duct dysplasia in lacrimo-auriculo-dento-digital syndrome.

Journal: International journal of ophthalmology
Published: January 28, 2023

Lacrimo-auriculo-dento-digital syndrome with AIRE mutation: A case report.

Lacrimo-auriculo-dento-digital syndrome with AIRE mutation: A case report.

Journal: Journal of stomatology, oral and maxillofacial surgery
Published: July 18, 2022

Phenotypic spectrum of FGF10-related disorders: a systematic review.

Phenotypic spectrum of FGF10-related disorders: a systematic review.

Journal: PeerJ
Published: June 03, 2022

Deletion of the last two exons of FGF10 in a family with LADD syndrome and pulmonary acinar hypoplasia.

Deletion of the last two exons of FGF10 in a family with LADD syndrome and pulmonary acinar hypoplasia.

Journal: European journal of human genetics : EJHG
Published: February 01, 2021

An Essential Requirement for Fgf10 in Pinna Extension Sheds Light on Auricle Defects in LADD Syndrome.

An Essential Requirement for Fgf10 in Pinna Extension Sheds Light on Auricle Defects in LADD Syndrome.

Journal: Frontiers in cell and developmental biology
Published: September 23, 2020

Lacrimo-auriculo-dento-digital syndrome: A case report and literature review.

Lacrimo-auriculo-dento-digital syndrome: A case report and literature review.

Journal: Saudi journal of ophthalmology : official journal of the Saudi Ophthalmological Society
Published: April 26, 2020
Showing 1-12 of 76

Last Updated: 04/28/2026