Congenital lymphedema and distichiasis

Pediatric Dermatology

Volumn 19, Issue 2, 2002, Pages 139-141

  Samlaska, Curt P ^a  

^a ROSEMAN UNIVERSITY OF HEALTH SCIENCES   (United States)

Author keywords

[No Author keywords available]

Indexed keywords

ARTICLE; AUTOSOMAL DOMINANT DISORDER; CASE REPORT; CAUCASIAN; CLINICAL FEATURE; DISTICHIASIS; EYELASH; GENE MUTATION; GENETIC ANALYSIS; HAIR DISEASE; HUMAN; INHERITANCE; INTRAUTERINE INFECTION; MALE; MILROY DISEASE; PRIORITY JOURNAL; SCHOOL CHILD; SPONTANEOUS MUTATION;

ABNORMALITIES, MULTIPLE; CHILD, PRESCHOOL; EYELASHES; HUMANS; LYMPHEDEMA; MALE;

EID: 0036257840     PISSN: 07368046     EISSN: None     Source Type: Journal    
DOI: 10.1046/j.1525-1470.2002.00048.x     Document Type: Article

References (14)

1. Lymphedema-distichiasis syndrome: Report of a case and review
2. Distichiasis-lympedema syndrome: Tetralogy of Fallot, chylothorax, and neonatal death
3. Distichiasis-lymphoedema syndrome: A family report
4. Primary lymphoedema when found with distichiasis is of the type defined as bilateral hyperplasia by lymphography
5. Hereditary spinal arachnoid cysts, distichiasis, and lymphedema
6. Syndrome of lymphoedema and distichiasis
7. Distichiasis-lymphedema: Clinical features, venous function and lymphoscintigraphy
8. Blepharocheilo-dontic (BCD) syndrome
9. Observations on distichiasis, telecanthus, ectropion and blow-out orbital fracture
10. Mutations in FOXC2 (MFH-1), a forkhead family transcription factor, are responsible for the hereditary lymphedema-distichiasis syndrome
11. A gene for lymphedema-distichiasis maps to 16q24.3
12. Distichiasis
13. Distichiasis complicating allergic rhinoconjunctivitis
14. Diseases of the eyelid-conjunctival complex and corneal complications of lid disease