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Pettigrew syndrome

Just diagnosed with Pettigrew syndrome?

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

Open the full Pettigrew syndrome hub →

Overview

Pettigrew syndrome is a rare condition. Also known as Pettigrew Syndrome, AP1S2-related neurodevelopmental disorder, AP1S2-related X-linked intellectual disability. Tomeko brings together the specialists, research, clinical trials, treatments and community for Pettigrew syndrome so you can go from overwhelmed to oriented. For authoritative medical detail, see the reference sources below.

Identifiers: ORPHA:1568 · OMIM 304340 · ICD-10 Q04.8 · GARD 0008520

Find care for Pettigrew syndrome

Authoritative references for Pettigrew syndrome

Common questions

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

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

Where can I find a specialist for Pettigrew syndrome?

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

Are there clinical trials for Pettigrew syndrome?

Tomeko shows live, recruiting studies for Pettigrew 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