You are not alone. Here is where to start: learn the basics, find a specialist or center that sees RIN2 syndrome, look for clinical trials, and connect with others living with it — all in one place.
Open the full RIN2 syndrome hub →RIN2 syndrome is a rare condition. Also known as MACS syndrome, Macrocephaly-alopecia-cutis laxa-scoliosis syndrome, RIN2 deficiency, Tall forehead-sparse hair-skin hyperextensibility-scoliosis syndrome. Tomeko brings together the specialists, research, clinical trials, treatments and community for RIN2 syndrome so you can go from overwhelmed to oriented. For authoritative medical detail, see the reference sources below.
Identifiers: ORPHA:217335 · OMIM 613075 · ICD-10 Q82.8 · GARD 0017120
Start by learning the basics from an authoritative source, find a specialist or center that sees RIN2 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 RIN2 syndrome, filtered to your area.
Tomeko shows live, recruiting studies for RIN2 syndrome from ClinicalTrials.gov on the hub.