Dyschromia, hereditary, familial, spottyL81.8
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Autosomal dominant inherited pigment disorder with multiple, blurred, irregularly arranged, hyper- and hypopigmented skin areas. Simultaneously: White forelock.
Differential diagnosisThis section has been translated automatically.
TherapyThis section has been translated automatically.
For cosmetic reasons, covering the skin spots (e.g. Dermacolor) or dyeing the hair.
LiteratureThis section has been translated automatically.
- Foldes C et al (1987) Congenital dyschromia. Ann Dermatol Venerol 114: 1267-1276