Macules hereditary congenital hypopigmented and hyperpigmented
Don’t fight Macules hereditary congenital hypopigmented and hyperpigmented alone.
Find your community on the free RareGuru App.Connect with other caregivers and patients with Macules hereditary congenital hypopigmented and hyperpigmented and get the support you need.
Description
The following summary is from Orphanet, a European reference portal for information on rare diseases and orphan drugs.
Orpha Number: 2435
Definition
Hypo- and hypermelanotic cutaneous macules-retarded growth-intellectual disability syndrome is a rare, genetic pigmentation anomaly of the skin disorder characterized by congenital hypomelanotic and hypermelanotic cutaneous macules associated with, in some patients, retarded growth and intellectual disability. There have been no further descriptions in the literature since 1978.
Visit the Orphanet disease page for more resources.
Source: GARD Last updated on 05-01-20
Symptoms
Symptoms and their Known Frequencies
Connect with other users with Macules hereditary congenital hypopigmented and hyperpigmented on the RareGuru app
Do you have information about a disease, disorder, or syndrome? Want to suggest a symptom?
Please send suggestions to RareGuru!
