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Hypopigmentation of the skin

A condition caused by a deficiency or a loss of melanin pigmentation in the epidermis, also known as hypomelanosis. Hypopigmentation can be localized or generalized, and may result from genetic defects, trauma, inflammation, or infections.

2 trials tagged with this condition →

Syndromic oculocutaneous albinism 0 trials · 12 incl. sub-types Sub-types →
Oculocutaneous albinism 4 trials Sub-types →
Piebaldism 4 trials
Tietz syndrome 1 trial
Ito hypomelanosis 0 trials
Albinism-hearing loss syndrome 0 trials
Deaf blind hypopigmentation syndrome, Yemenite type 0 trials
Deafness, congenital, with total albinism 0 trials
Linear hypopigmentation and craniofacial asymmetry with acral, ocular and brain anomalies 0 trials
Piebald trait-neurologic defects syndrome 0 trials