Mesh term Werner Syndrome
Browse to parent terms:DNA Repair-Deficiency Disorders
Genetic Diseases, Inborn
Description
An autosomal recessive disorder that causes premature aging in adults, characterized by sclerodermal skin changes, cataracts, subcutaneous calcification, muscular atrophy, a tendency to diabetes mellitus, aged appearance of the face, baldness, and a high incidence of neoplastic disease.Search for this term in our Faculty Database
View this term at the NCBI website
