You are not alone. Here is where to start: learn the basics, find a specialist or center that sees Neu-Laxova syndrome 1, look for clinical trials, and connect with others living with it — all in one place.
Open the full Neu-Laxova syndrome 1 hub →Neu-Laxova syndrome 1 is a rare condition. Also known as 3-phosphoglycerate dehydrogenase deficiency, prenatal form. Tomeko brings together the specialists, research, clinical trials, treatments and community for Neu-Laxova syndrome 1 so you can go from overwhelmed to oriented. For authoritative medical detail, see the reference sources below.
Identifiers: ORPHA:583607 · OMIM 256520 · ICD-10 Q87.8 · GARD 0022336
Start by learning the basics from an authoritative source, find a specialist or center that sees Neu-Laxova syndrome 1, and connect with a patient organization. Tomeko brings these together on one hub.
Use Tomeko's specialist and Centers-of-Excellence directories to find clinicians who treat Neu-Laxova syndrome 1, filtered to your area.
Tomeko shows live, recruiting studies for Neu-Laxova syndrome 1 from ClinicalTrials.gov on the hub.