| Item | Content |
|---|---|
| Research project name | Practical Research Project for Rare / Intractable Diseases |
| Study title | Development of evidence through the nation-wide survey on progeroid Werner syndrome and establishment of the case registration system |
| Name of principal investigator | Koutaro Yokote |
| Name of institution of the principal investigator | Clinical Cell Biology and Medicine, Chiba University Graduate School of Medicine |
| Target disease | Werner syndrome |
| Registry name | Werner syndrome registry |
| Purpose of registry | Survey of natural history, Investigation into the number or the distribution of patients, Epidemiological study, Patient recruitment for clinical trials or other interventional studies, Sample collection, Genetic analysis study, Provision of information to registered patients, Provision of information to physicians in charge |
| Overview of registry | - Collection of epidemiological information on Werner syndrome (e.g., patient distribution, prognosis, prognostic factors, disease type) - Recruitment of subjects for the clinical trial on Werner syndrome, e.g. “development of a treatment drug for intractable ulcers in patients with inherited progeria by new peptides with antimicrobial activity and wound repair action” and “development of evidence by establishment of iPS cells derived from patients with progeroid syndrome” - Information dissemination basis for patients with Werner syndrome |
| Research item | Sex, Date of birth, Past medical history, Complication, History of present illness, History of treatment, Laboratory data |
| Contact | Masaya Koshisaka |
| E-mail address | overslope●chiba-u.jp |
| Registry URL | http://www.m.chiba-u.jp/class/clin-cellbiol/werner/ |
* If the E-mail address is shown, replace "●" with "@", please.