Hemihyperplasia-multiple lipomatosis syndrome

Diseases of the skin and subcutaneous tissue

rare capillary malformation with associated anomalies; rare genetic bone disease; genetic skin vascular disorder; syndrome or malformation associated with head and neck malformations; skull cancer; malformation syndrome with hamartosis; skin tumor or hamartoma; rare genetic vascular tumor; overgrowt

A rare, genetic overgrowth syndrome characterized by non- progressive, asymmetrical, moderate hemihyperplasia (frequently affecting the limbs) associated with slow growing, painless, multiple, recurrent, subcutaneous lipomatous masses distributed throughout entire body (in particular back, torso, extremities, fingers, axillae).