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Last Updated: 10/31/2025
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Found 52 publications
Clinical features and genetic analysis of two Chinese pedigrees affected with Lymphedema-Distichiasis syndrome
Journal: Zhonghua yi xue yi chuan xue za zhi = Zhonghua yixue yichuanxue zazhi = Chinese journal of medical genetics
Published: December 09, 2024
Generation of human induced pluripotent stem cell line from peripheral blood of patient with lymphedema-distichiasis syndrome.
Journal: Stem cell research
Published: April 05, 2024
Ophtalmologic diagnosis of lymphedema-distichiasis syndrome through the FOXC2 mutation.
Journal: Archivos de la Sociedad Espanola de Oftalmologia
Published: May 30, 2023
Genetic landscape of FOXC2 mutations in lymphedema-distichiasis syndrome: Different mechanism of pathogenicity for mutations in different domains.
Journal: Experimental eye research
Published: April 27, 2022
Distichiasis: An update on etiology, treatment and outcomes.
Journal: Indian journal of ophthalmology
Published: March 25, 2022
Retrograde lymph flow in the lymphatic vessels in limb lymphedema.
Journal: Journal of vascular surgery. Venous and lymphatic disorders
Published: January 05, 2022
Compound genetic etiology in a patient with a syndrome including diabetes, intellectual deficiency and distichiasis.
Journal: Orphanet journal of rare diseases
Published: August 25, 2021
Microdeletion of 16q24.1-q24.2-A unique etiology of Lymphedema-Distichiasis syndrome and neurodevelopmental disorder.
Journal: American journal of medical genetics. Part A
Published: April 01, 2021
Genetic analysis and clinical phenotype of a family with lymphedema-distichiasis syndrome
Journal: Zhejiang da xue xue bao. Yi xue ban = Journal of Zhejiang University. Medical sciences
Published: November 19, 2020
FOXC2 Disease Mutations Identified in Lymphedema Distichiasis Patients Impair Transcriptional Activity and Cell Proliferation.
Journal: International journal of molecular sciences
Published: June 08, 2020
Lymphedema distichiasis syndrome may be caused by FOXC2 promoter-enhancer dissociation and disruption of a topological associated domain.
Journal: American journal of medical genetics. Part A
Published: May 23, 2020
Last Updated: 10/31/2025