Congenital lymphedema in Infant/Neonate
Congenital lymphedema is caused by a mutation in the FLT4 gene, which encodes the vascular endothelial growth factor receptor 3 (VEGFR-3), that leads to aplasia or hypoplasia of lymphatic channels. It is inherited in an autosomal dominant fashion and presents with lymphedema that develops before the age of 2. It is typically present from birth or shortly thereafter and may be either bilateral or asymmetric. At first, the dorsal feet are edematous. As the child grows, this may progressively involve the entire lower leg. The degree and distribution of the edema can vary widely from case to case, even among individuals of the same family.
Lymphedema does not usually affect longevity, and serious complications of lymphedema are rare, but lasting and/or bothersome cosmetic imperfections are experienced, as well as functional impairment. Complications include recurrent cellulitis, lymphangitis, and deep venous thrombosis. People with chronic lymphedema have a higher risk of developing lymphangiosarcoma, a highly aggressive angiosarcoma with poor prognosis.
Other associations include hydrocele and urethral abnormalities in males, such as urethral stricture or hypospadias. Prominent lower extremity veins and hemangiomas may be seen.
Atypical presentations of Milroy disease secondary to de novo VEGFR-3 mutations may include prenatal pleural effusion, spontaneous resorption of lymphedema, and elephantiasis.
The overall prevalence is unknown.
Q82.0 – Hereditary lymphedema
399889006 – Hereditary lymphedema type I
- Multisegmental lymphatic dysplasia with systemic involvement
- Generalized lymphatic dysplasia (Hennekam syndrome)
- Proteus syndrome
- CLOVE syndrome / fibroadipose hyperplasia
- Klippel-Trenaunay syndrome
- Parkes-Weber syndrome
- Combined vascular malformation
- Lymphangiomatosis / Gorham disease
- Warts, immunodeficiency, lymphedema, anogenital dysplasia (WILD) syndrome