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Kindler syndrome

Just diagnosed with Kindler syndrome?

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

Open the full Kindler syndrome hub →

Overview

Kindler syndrome is a rare condition. Also known as Congenital bullous poikiloderma, Kindler syndrome, Poikiloderma of Kindler. Tomeko brings together the specialists, research, clinical trials, treatments and community for Kindler syndrome so you can go from overwhelmed to oriented. For authoritative medical detail, see the reference sources below.

Identifiers: ORPHA:2908 · OMIM 173650 · ICD-10 Q81.8 · GARD 0004391

Find care for Kindler syndrome

Authoritative references for Kindler syndrome

Common questions

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

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

Where can I find a specialist for Kindler syndrome?

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

Are there clinical trials for Kindler syndrome?

Tomeko shows live, recruiting studies for Kindler 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