Abstract:
CLOVES syndrome is a rare, newly described, and relatively unknown syndrome, related to somatic mutations of the PIK3CA gene. Clinical findings include adipose tissue overgrowth, vascular malformations, epidermal nevi, scoliosis, and spinal deformities. This report deals with a characteristic phenotype case, highlighting peculiar cutaneous and radiological changes.
Keywords:
Adipose tissue; Klippel-Trenaunay-Weber Syndrome; Proteus Syndrome; Vascular Malformations
