Syndrome

Weill-Marchesani Syndrome

AMW:DIS:050014

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.

Pathology clinical

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Weill-Marchesani Syndrome has parent Abnormalities, Multiple

Weill-Marchesani Syndrome has parent Connective Tissue Diseases

Weill-Marchesani Syndrome has parent Dwarfism

Weill-Marchesani Syndrome has parent Eye Diseases, Hereditary

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