Microspherophakia or Weill Marchesani Syndrome (Q84041): Difference between revisions
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Revision as of 09:24, 15 August 2026
Weill-Marchesani syndrome (WMS) is a rare inherited syndrome characterised by short stature, brachydactyly, joint stiffness, and characteristic eye abnormalities including microspherophakia, ectopia of the lens, severe myopia, and glaucoma.
| Language | Label | Description | Also known as |
|---|---|---|---|
| default for all languages | ID_1683934843 |
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| English | Microspherophakia or Weill Marchesani Syndrome |
Weill-Marchesani syndrome (WMS) is a rare inherited syndrome characterised by short stature, brachydactyly, joint stiffness, and characteristic eye abnormalities including microspherophakia, ectopia of the lens, severe myopia, and glaucoma. |
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CID11:ID_1683934843
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dki-india-ID_1683934843
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