OMIM
Weill-Marchesani syndrome is a rare connective tissue disorder characterized by short stature, brachydactyly, joint stiffness, eye anomalies, including microspherophakia, ectopia of the lenses, severe myopia, and glaucoma, and, occasionally, heart defects (summary by Dagoneau et al., 2004). (277600)
Information about
| Nume | Weill-Marchesani Syndrome 1 | |
|---|---|---|
| Pagina Web | www.malacards.org | |
| Clasificare globală Malacards | Fetal diseases; Genetic diseases; Rare diseases | |
| Clasificare anatomică Malacards | Bone diseases; Eye diseases; Skin diseases | |
| Boli din aceeaşi familie | Weill-Marchesani Syndrome 2; Weill-Marchesani Syndrome 3; Weill-Marchesani-Like Syndrome |