hereditary lymphedema IA

A hereditary lymphedema characterized by autosomal dominant inheritance that has_material_basis_in mutation in the FLT4 gene on chromosome 5q35.

Signs and symptoms

• Hypoplasia of lymphatic vessels
• Predominantly lower limb lymphedema
• Hyperkeratosis over edematous areas
• Hemangioma
• Hydrocele testis
• Prominent superficial veins
• Cellulitis
• Upslanting toenail
• Papilloma
• Urethral stricture

Also known as: LMPH1A