Incontinentia pigmenti
MONDO:0010631Incontinentia pigmenti (IP) is a rare X-linked dominant multi-systemic ectodermal dysplasia usually lethal in males and presenting neonatally in females with a bullous rash along Blashko's lines (BL) followed by verrucous plaques evolving over time to hyperpigmented swirling patterns. It is further characterized by teeth abnormalities, alopecia, nail dystrophy and affects occasionally the retina and the central nervous system (CNS).
Also known as: Bloch-Siemens syndrome, Bloch-Sulzberger syndrome, Incontinentia pigmenti syndrome, incontinentia pigmenti, incontinentia pigmenti, X-linked dominant, IP, IP2 (formerly), Incontinentia pigmenti type 2 (formerly)
16 clinical trials for this condition and its sub-types, 3 tagged with Incontinentia pigmenti itself.
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Can a smartphone dashboard boost mental health care in rwanda?
Knowledge-focused Recruiting nowThis study tests a digital dashboard tool to help community workers deliver a family-based mental health program called Sugira Muryango in Rwanda. The goal is to see if the technology improves how well the program is delivered, including fidelity and worker confidence. Over 1,800…
Sponsor: Boston College • Aim: Knowledge-focused
Last updated Jun 27, 2026 12:01 UTC
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New study to measure hidden toll of rare skin diseases on patients and families
Knowledge-focused Recruiting nowThis study aims to understand the full burden of 9 rare skin diseases—including physical, emotional, social, and financial challenges—on patients and their families. Researchers will use special questionnaires to track how these conditions affect daily life and care needs. About …
Sponsor: Institut National de la Santé Et de la Recherche Médicale, France • Aim: Knowledge-focused
Last updated Jun 27, 2026 09:04 UTC