You are not alone. Here is where to start: learn the basics, find a specialist or center that sees Cutis laxa with severe pulmonary, gastrointestinal and urinary anomalies, look for clinical trials, and connect with others living with it — all in one place.
Open the full Cutis laxa with severe pulmonary, gastrointestinal and urinary anomalies hub →Cutis laxa with severe pulmonary, gastrointestinal and urinary anomalies is a rare condition. Also known as ARCL1C, Autosomal recessive cutis laxa type 1C, Urban-Rifkin-Davis syndrome. Tomeko brings together the specialists, research, clinical trials, treatments and community for Cutis laxa with severe pulmonary, gastrointestinal and urinary anomalies so you can go from overwhelmed to oriented. For authoritative medical detail, see the reference sources below.
Identifiers: ORPHA:221145 · OMIM 613177 · ICD-10 Q82.8 · GARD 0017140
Start by learning the basics from an authoritative source, find a specialist or center that sees Cutis laxa with severe pulmonary, gastrointestinal and urinary anomalies, 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 Cutis laxa with severe pulmonary, gastrointestinal and urinary anomalies, filtered to your area.
Tomeko shows live, recruiting studies for Cutis laxa with severe pulmonary, gastrointestinal and urinary anomalies from ClinicalTrials.gov on the hub.