Disease: Distichiasis heart congenital anomalies
- A case of lymphedema-distichiasis syndrome carrying a new de novo frameshift FOXC2 mutation
- A new classification system for primary lymphatic dysplasias based on phenotype
- Analysis of the phenotypic abnormalities in lymphoedema-distichiasis syndrome in 74 patients with FOXC2 mutations or linkage to 16q24
- c. 595-596 insC of FOXC2 underlies lymphedema, distichiasis, ptosis, ankyloglossia, and Robin sequence in a Thai patient
- Comparative lymphatic, ocular, and metabolic phenotypes of Foxc2 haploinsufficient and aP2-FOXC2 transgenic mice
- Distichiasis-lymphedema syndrome
- Distichiasis-lymphedema syndrome: tetralogy of Fallot, chylothorax, and neonatal death
- Distichiasis, congenital heart defects and mixed peripheral vascular anomalies
- Foxc2 influences alveolar epithelial cell differentiation during lung development
- FOXC2 truncating mutation in distichiasis, lymphedema, and cleft palate
- Index of suspicion
- Lymphedema in a patient with distichiasis
- Lymphedema-Distichiasis Syndrome
- Lymphedema-distichiasis syndrome: a distinct type of primary lymphedema caused by mutations in the FOXC2 gene
- Lymphoedema - distichiasis syndrome with recurrent abortions
- Lymphoscintigraphic Abnormalities Associated with Milroy Disease and Lymphedema-Distichiasis Syndrome
- Perinatal diagnosis of a lymphedema-distichiasis syndrome (LD)
- Pigmentary mosaicism as a recurrent clinical manifestation in three new patients with mosaic trisomy 12 diagnosed postnatally: cases report and literature review
- Renal anomalies and lymphedema distichiasis syndrome. A rare association?
- Variants in members of the cadherin-catenin complex, CDH1 and CTNND1, cause blepharocheilodontic syndrome