• A case of lymphedema-distichiasis syndrome carrying a new de novo frameshift FOXC2 mutation
• A peculiar syndrome of congenital abnormalities
• Advancement of the frontalis muscle for ptosis of the brow associated with essential blepharospasm
• AIDS-Related Kaposi Sarcoma Associated with Steroid-Unresponsive Periorbital Lymphedema that Responded to Chemotherapy
• Analysis of the phenotypic abnormalities in lymphoedema-distichiasis syndrome in 74 patients with FOXC2 mutations or linkage to 16q24
• Autosomal or X-linked recessive syndrome of congenital lymphedema, hypoparathyroidism, nephropathy, prolapsing mitral valve, and brachytelephalangy
• Blepharochalasis. A review of 30 cases
• c. 595-596 insC of FOXC2 underlies lymphedema, distichiasis, ptosis, ankyloglossia, and Robin sequence in a Thai patient
• Case Series of Morbihan Disease (Extreme Eyelid Oedema Associated with Rosacea): Diagnostic and Therapeutic Approaches
• Clinical heterogeneity in lymphoedema-distichiasis with FOXC2 truncating mutations
• Complications in Brachioplasty: A Systematic Review and Meta-Analysis
• Complications of radical vulvectomy and adjacent lymphadenectomy based on 58 cases of vulvar cancer
• Distichiasis of the lids and lymphedema of the lower extremities: a report of ten cases
• Distichiasis-lymphedema syndrome and the Turner phenotype
• Elephantoid oedema of the eyelids
• Expansion of the phenotype in Hennekam syndrome: a case with new manifestations
• Eye symptoms in connatal lymphedema
• Genetic diseases affecting the eyelids: what should a clinician know?
• Germline CBL mutation associated with a noonan-like syndrome with primary lymphedema and teratoma associated with acquired uniparental isodisomy of chromosome 11q23
• Late radiation side effects, cosmetic outcomes and pain in breast cancer patients after breast-conserving surgery and three-dimensional conformal radiotherapy : Risk-modifying factors
• Lymphangiosarcoma in a 3.5-year-old Bullmastiff bitch with vaginal prolapse, primary lymph node fibrosis and other congenital defects
• 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
• Mastopexy for breast ptosis: Utility outcomes of population preferences
• Medial thigh lift in post-bariatric patients: Our encouraging experience
• Molecular genetics of Turner syndrome: correlation with clinical phenotype and response to growth hormone therapy
• Novel FOXC2 Mutation in Hereditary Distichiasis Impairs DNA-Binding Activity and Transcriptional Activation
• Persistent periorbital and facial lymphedema associated with Group A beta-hemolytic streptococcal infection (erysipelas)
• Prenatal diagnosis of Milroy's primary congenital lymphedema
• Primary non-syndromic lymphoedema (Meige disease) is not caused by mutations in FOXC2
• Ptosis with elephantiasis and ectropion
• Renal anomalies and lymphedema distichiasis syndrome. A rare association?
• Rosacea lymphoedema of the eyelid
• Silicone oil migration in the eyelid after vitrectomy for retinal detachment
• Syndrome of lymphoedema and distichiasis
• The basics of baggy eyelids
• The Posterior Arm Flap for Reshaping the Postbariatric Breast
• Two case presentations of profound labial edema as a presenting symptom of hypermobility-type Ehlers-Danlos syndrome