Psoriasis is an immune-mediated disease that causes inflammation in the body and is associated with visible signs of the inflammation [...]
Tuberous sclerosis (TSC) is a genetic disorder that causes tumors to form in various organs, primarily the brain, heart, kidney, [...]
Vitiligo is an autoimmune skin condition in which there is loss of pigment from areas of the skin resulting in [...]
PHACE Syndrome is the uncommon association between large infantile hemangiomas, usually of the face, and birth defects of the brain, [...]
Ichthyosis is a family of genetic skin disorders characterized by dry, scaling skin that may be thickened or very thin.
Albinism is a recessive genetic condition that causes the absence or reduction of pigmentation in the hair, skin and eyes.
CFC syndrome is a rare genetic condition that typically affects the heart (cardio), facial features (facio) and skin (cutaneous). Children [...]
CLOVES Syndrome stands for Congenital, Lipomatous, Overgrowth, Vascular Malformations, Epidermal Nevi and Spinal/Skeletal Anomalies and/or Scoliosis and was identified simultaneously [...]