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. | |||
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 |
|---|---|---|---|
| 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. |
