Mesh term Weill-Marchesani Syndrome
Browse to parent terms:Abnormalities, Multiple
Connective Tissue Diseases
Dwarfism
Eye Diseases, Hereditary
Description
Rare congenital disorder of connective tissue characterized by brachydactyly, joint stiffness, childhood onset of ocular abnormalities (e.g., microspherophakia, ECTOPIA LENTIS; GLAUCOMA), and proportionate short stature. Cardiovascular anomalies are occasionally seen.Search for this term in our Faculty Database
View this term at the NCBI website
