Peters anomaly (Q59343): Difference between revisions

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Property / Canonical URI: https://id.who.int/icd/entity/1902926622 / rank
 
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CID11:ID_1902926622
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dki-india-ID_1902926622
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Concluído
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Property / Knowledge Architect: https://pauloleads.com.br/cases-publicos/ / rank
 
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13 August 2026
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Latest revision as of 06:52, 14 August 2026

Peters anomaly, or Peters congenital glaucoma, is a genetic eye developmental disorder characterised by trabecular dysgenesis that causes glaucoma, which is generally bilateral. Descemet's membrane and the endothelium at the centre of the cornea fail to develop, leading to opacities in the central cornea with iridocorneal synechia that stretch from the edge of the irides to the central opacity. The anterior chamber is narrow and may adhere to the lens. Cataract can be associated.
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ID_1902926622
    English
    Peters anomaly
    Peters anomaly, or Peters congenital glaucoma, is a genetic eye developmental disorder characterised by trabecular dysgenesis that causes glaucoma, which is generally bilateral. Descemet's membrane and the endothelium at the centre of the cornea fail to develop, leading to opacities in the central cornea with iridocorneal synechia that stretch from the edge of the irides to the central opacity. The anterior chamber is narrow and may adhere to the lens. Cataract can be associated.

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      CID11:ID_1902926622
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      dki-india-ID_1902926622
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      Concluído
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      13 August 2026
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