Microspherophakia or Weill Marchesani Syndrome (Q84041): Difference between revisions
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Síndrome de Weill-Marchesani (WMS) é uma síndrome hereditária rara caracterizada por baixa estatura, braquidactilia, rigidez articular e anormalidades oculares características, incluindo microesferofacia, ectopia do cristalino, miopia grave e glaucoma. | |||
| description / en | description / en | ||
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. | |||
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 |
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| 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. |
