You are not alone. Here is where to start: learn the basics, find a specialist or center that sees Laron-type isolated somatotropin defect, look for clinical trials, and connect with others living with it — all in one place.
Open the full Laron-type isolated somatotropin defect hub →Laron-type isolated somatotropin defect is a rare condition. Also known as Complete growth hormone insensitivity, GH receptor deficiency, Growth hormone receptor deficiency, Laron-type dwarfism, Primary GH insensitivity, Primary GH resistance, Primary growth hormone insensitivity, Primary growth hormone resistance. Tomeko brings together the specialists, research, clinical trials, treatments and community for Laron-type isolated somatotropin defect so you can go from overwhelmed to oriented. For authoritative medical detail, see the reference sources below.
Identifiers: ORPHA:633 · OMIM 262500 · ICD-10 E34.3 · GARD 0006859
Start by learning the basics from an authoritative source, find a specialist or center that sees Laron-type isolated somatotropin defect, 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 Laron-type isolated somatotropin defect, filtered to your area.
Tomeko shows live, recruiting studies for Laron-type isolated somatotropin defect from ClinicalTrials.gov on the hub.