Alport syndrome (Q54857): Difference between revisions
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A síndrome de Alport é uma doença hereditária caracterizada por nefropatia glomerular com hematúria, que evolui para doença renal em estágio terminal, associada a surdez neurossensorial e condições oculares como lenticone ou retinopatia. Envolve um defeito estrutural do colágeno tipo IV, que é um componente normal da membrana basal glomerular. | |||||||||||||||
| description / en | description / en | ||||||||||||||
Alport syndrome is an inherited disease characterised by glomerular nephropathy with haematuria, progressing to end-stage renal disease, associated with sensorineural deafness and eye affection such as lenticonus or retinopathia. It involves a structural defect of type IV collagen, which is a normal component of the glomeral basal membrane. | |||||||||||||||
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| Property / Canonical URI: https://id.who.int/icd/entity/1170919425 / rank | |||||||||||||||
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CID11:ID_1170919425 | |||||||||||||||
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dki-india-ID_1170919425 | |||||||||||||||
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| Property / Verification Status: Concluído / rank | |||||||||||||||
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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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| Property / Collection date: 13 August 2026 / rank | |||||||||||||||
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Latest revision as of 02:29, 14 August 2026
Alport syndrome is an inherited disease characterised by glomerular nephropathy with haematuria, progressing to end-stage renal disease, associated with sensorineural deafness and eye affection such as lenticonus or retinopathia. It involves a structural defect of type IV collagen, which is a normal component of the glomeral basal membrane.
| Language | Label | Description | Also known as |
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| default for all languages | ID_1170919425 |
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| English | Alport syndrome |
Alport syndrome is an inherited disease characterised by glomerular nephropathy with haematuria, progressing to end-stage renal disease, associated with sensorineural deafness and eye affection such as lenticonus or retinopathia. It involves a structural defect of type IV collagen, which is a normal component of the glomeral basal membrane. |
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CID11:ID_1170919425
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dki-india-ID_1170919425
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Concluído
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13 August 2026
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