Incontinentia pigmenti is a rare genodermatosis that usually affects female infants.The associated abnormalities involve ocular, dental, skeletal and central nervous systems.
Hay-Wells Syndrome (HWS), also known as the ankyloblepharon-ectodermal dysplasia-clefting (AEC) syndrome, is one of at least 150 known types of ectodermal dysplasia.
Galactosemia is another rare metabolic disorder that occurs when the liver enzyme GALT, needed to break down galactose, is partially or completely absent.
Systemic mastocytosis results in the accumulation of mast cells in various tissues.We report a rare case of systemic mastocytosis presenting with cholestatic liver disease.
This paper is reported a rare case of palmoplanter keratoma hereditaria-keratoma hereditaria mutilans and differential diagnosis with various palmoplantar keratodermas and dactylolysis are discussed.