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Incontinentia pigmenti syndrome

Just diagnosed with Incontinentia pigmenti syndrome?

You are not alone. Here is where to start: learn the basics, find a specialist or center that sees Incontinentia pigmenti syndrome, look for clinical trials, and connect with others living with it — all in one place.

Open the full Incontinentia pigmenti syndrome hub →

Overview

Incontinentia pigmenti syndrome is a rare condition. Also known as Bloch-Siemens syndrome, Bloch-Sulzberger syndrome. Tomeko brings together the specialists, research, clinical trials, treatments and community for Incontinentia pigmenti syndrome so you can go from overwhelmed to oriented. For authoritative medical detail, see the reference sources below.

Identifiers: ORPHA:464 · OMIM 308300 · ICD-10 Q82.3 · GARD 0006778

Find care for Incontinentia pigmenti syndrome

Authoritative references for Incontinentia pigmenti syndrome

Common questions

I was just diagnosed with Incontinentia pigmenti syndrome — what should I do first?

Start by learning the basics from an authoritative source, find a specialist or center that sees Incontinentia pigmenti syndrome, and connect with a patient organization. Tomeko brings these together on one hub.

Where can I find a specialist for Incontinentia pigmenti syndrome?

Use Tomeko's specialist and Centers-of-Excellence directories to find clinicians who treat Incontinentia pigmenti syndrome, filtered to your area.

Are there clinical trials for Incontinentia pigmenti syndrome?

Tomeko shows live, recruiting studies for Incontinentia pigmenti syndrome from ClinicalTrials.gov on the hub.

Informational only — not medical advice. Always consult a qualified clinician. Provider and reference data from public sources (NIH GARD, Orphanet, OMIM, HPO, MONDO, ClinicalTrials.gov, CMS NPPES). © Tomeko · tomekohealth.com