Condition
Weill-Marchesani Syndrome
Dermatology
Overview
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.
This information is general and should not be treated as medical advice. Always speak directly with a qualified healthcare professional before making decisions about treatment, diagnosis, procedures, medicines or care.
Quick facts about Weill-Marchesani Syndrome
- Topic type
- Condition
- Category
- Dermatology
- MeSH classification
- C05.116.099.343.957|C11.270.921|C16.131.077.941|C16.320.290.842|C17.300.899
Preparing for an appointment about Weill-Marchesani Syndrome
If you are speaking with a healthcare professional about Weill-Marchesani Syndrome, it can help to prepare a few details in advance.
- Write down your symptoms and when they started.
- Bring details of any medicines, supplements or previous treatments.
- Ask what tests or assessments may be needed.
- Ask what treatment or management options may be suitable.
- Ask when you should seek urgent medical help or follow-up care.
Finding care related to Weill-Marchesani Syndrome
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Source: Medical Subject Headings (MeSH), produced by the U.S. National Library of Medicine. EuroCareFinder is not endorsed by the National Library of Medicine. MeSH version: 2026.