Семейная прогрессирующая гипер- и гипопигментация

Familial progressive hyper- and hypopigmentation is a rare, genetic, skin pigmentation anomaly disorder characterized by progressive, diffuse, partly blotchy, hyperpigmented lesions that are intermixed with multiple cafÚ-au-lait spots, hypopigmented maculae and lentigines and are located on the face, neck, trunk and limbs, as well as, frequently, the palms, soles and oral mucosa. Dispigmentation pattern can range from well isolated cafÚ-au-lait/hypopigmented patches on a background of normal-appearing skin to confetti-like or mottled appearance.