You are not alone. Here is where to start: learn the basics, find a specialist or center that sees Kostmann syndrome, look for clinical trials, and connect with others living with it — all in one place.
Open the full Kostmann syndrome hub →Kostmann syndrome is a rare condition. Also known as Infantile agranulocytosis, Severe congenital neutropenia type 3. Tomeko brings together the specialists, research, clinical trials, treatments and community for Kostmann syndrome so you can go from overwhelmed to oriented. For authoritative medical detail, see the reference sources below.
Identifiers: ORPHA:99749 · OMIM 610738 · ICD-10 D70 · GARD 0000302
Start by learning the basics from an authoritative source, find a specialist or center that sees Kostmann syndrome, 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 Kostmann syndrome, filtered to your area.
Tomeko shows live, recruiting studies for Kostmann syndrome from ClinicalTrials.gov on the hub.