Dyschromia, hereditary, familial, spotty L81.8

Author: Prof. Dr. med. Peter Altmeyer

All authors of this article

Last updated on: 29.10.2020

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Definition
This section has been translated automatically.

Autosomal dominant inherited pigment disorder with multiple, blurred, irregularly arranged, hyper- and hypopigmented skin areas. Simultaneously: White forelock.

Differential diagnosis
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Klein-Waardenburg syndrome; Vitiligo; Piebaldism.

Therapy
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For cosmetic reasons, covering the skin spots (e.g. Dermacolor) or dyeing the hair.

Literature
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  1. Foldes C et al (1987) Congenital dyschromia. Ann Dermatol Venerol 114: 1267-1276

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Outgoing links (3)

Klein-waardenburg syndrome; Piebaldism; Vitiligo (overview);

Disclaimer

Please ask your physician for a reliable diagnosis. This website is only meant as a reference.

Authors

Last updated on: 29.10.2020

Author: Prof. Dr. med. Peter Altmeyer Prof. Dr. med. Peter Altmeyer

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