A genetic disorder with two distinct features: persistent, figurate, red-brown hyperkeratotic plaques and transient, migratory annular erythematous patches.
A syndrome known as KID syndrome, characterized by vascularizing keratitis of the eyes, hyperkeratotic skin plaques, and sensorineural deafness.
A genetic disorder with fixed, well-demarcated, symmetric, erythematous, and hyperkeratotic plaques on the extremities, buttocks, and face.
