dyschromatosis symmetrica hereditaria
MeSH: C535729ORPHA: 41
Overview
pigmentation disease characterized by progressively pigmented and depigmented macules, often mixed in a reticulate pattern, concentrated on the dorsal extremities
Available Treatments (0)
No treatments linked yet
Clinical trials or compassionate use may be available — consult a specialist.
Clinical Presentation
Signs and symptoms associated with dyschromatosis symmetrica hereditaria, sourced from HPO and Orphanet clinical annotations.
Torsion dystoniaMacular hypopigmentationMacular hyperpigmentationMacule
Classification & Codes
MeSH Code
C535729Orphanet Code
ORPHA:41dyschromatosis symmetrica hereditaria
| MeSH | C535729 |
| Orphanet | ORPHA:41 |
| Treatments | 0 drug(s) |
| Symptoms on record | 4 signs |
| Status | published |
Factual Authority
Last Updated3/20/2026
Clinical DataHPO · Orphanet
Drug DataFDA · EMA · CDSCO