Familial progressive hyperpigmentation
Other names	Melanosis universalis hereditaria[1]
This condition in inherited in an autosomal dominant manner
Specialty	Medical genetics

Familial progressive hyperpigmentation is characterized by patches of hyperpigmentation, present at birth, which increase in size and number with age. This is a genetic disease, however the gene that accounts for this spotty darkening of the skin has yet to be discovered. Although rare, the congenital disease is most prevalent among populations originating from China.^[2]: 858

See also

• Skin lesion

References

The American Journal of Human Genetics 84, 672–677, May 15, 2009

External links