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Piebaldism refers to the absence of mature melanin-forming cells (melanocytes) in certain areas of the skin and hair. It is a rare autosomal dominant disorder of melanocyte development. [ 2 ] : 867 Common characteristics include a congenital white forelock , scattered normal pigmented and hypopigmented macules and a triangular shaped ...
Some genetic conditions that result in a "leucistic" appearance include piebaldism, Waardenburg syndrome, vitiligo, Chédiak–Higashi syndrome, flavism, isabellinism, xanthochromism, axanthism, amelanism, and melanophilin mutations. Pale patches of skin, feathers, or fur (often referred to as "depigmentation") can also result from injury.
Dermatological signs such as hypomelanotic macules and facial angiofibromas are common, and poliosis can occasionally be an early indicator of TSC. [ 2 ] Piebaldism : This rare genetic disorder is characterized by a congenital absence of melanocytes in certain areas of the skin and hair, leading to white patches or forelocks.
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Vitiligo (/ ˌ v ɪ t ɪ ˈ l aɪ ɡ oʊ /, vit-il-eye-goh) is a chronic autoimmune disorder that causes patches of skin to lose pigment or color. [1] The cause of vitiligo is unknown, but it may be related to immune system changes, genetic factors, stress, or sun exposure. [5] [6] Treatment options include topical medications, light therapy ...
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Vitiligo: Topical steroids, including calcineurin inhibitors. Patients can also have transplants if they are stable or a depigmentation with topical MBEH if the patient has widespread discoloration. Chemical or drug induced leukoderma: Avoidance of causative agent with subsequent treatment similar to vitiligo. Piebaldism: None; occasionally ...
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