Cure My Disease

Don't miss your cure!

Home News Browse Soon ready About
Log in / Sign up

Piebaldism

MONDO:0008244

Piebaldism is a rare congenital pigmentation skin disorder characterized by the presence of hypopigmented and depigmented skin areas (leukoderma) on various parts of the body, preferentially on the forehead, chest, abdomen, upper arms, and lower extremities, that are associated with a white forelock (poliosis), and in some cases with hypopigmented and depigmented eyebrows and eyelashes.

Also known as: piebald trait, piebaldism, PBT

4 clinical trials for this condition and its sub-types.

Follow this condition — get notified about new trials

Broader categories

Disease (680) Hereditary disease (176) Skin disorder (132) Eye disorder (102) Human disease (14) Skin pigmentation disorder (11) Hereditary skin disorder (6) Disorder of orbital region (3) Disease of genetic or genomic mechanism (2) Hypopigmentation of the skin (2)
Trials to join now! 3 Not yet finished but already full! 1
Sort by
  • New study tests gentler tooth removal for faster implant healing

    Symptom relief Ongoing

    This study compares two tools, piezotome and periotome, used for gentle tooth extraction before placing a dental implant right away in the front upper teeth. The goal is to see which tool better preserves bone and gum tissue, leading to improved healing and appearance. Thirty adu…

    Phase: NA • Sponsor: Alexandria University • Aim: Symptom relief

    Last updated Jun 27, 2026 08:04 UTC

Cure My Disease

Helping patients find clinical trials that match their disease.

Why was Cure my disease built?

Explore

Home News Browse About Terms of use Contact us

This is a site from Cyber and Space