Congenital stationary night blindness (Q99765): Difference between revisions
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15 August 2026
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Latest revision as of 16:26, 16 August 2026
This is a rare X-linked non-progressive retinal disorder. It has two forms, complete, also known as type-1 (CSNB1), and incomplete, also known as type-2 (CSNB2), depending on severity. In the complete form (CSNB1), there is no measurable rod cell response to light, whereas this response is measurable in the incomplete form.
| Language | Label | Description | Also known as |
|---|---|---|---|
| default for all languages | ID_587494652 |
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| English | Congenital stationary night blindness |
This is a rare X-linked non-progressive retinal disorder. It has two forms, complete, also known as type-1 (CSNB1), and incomplete, also known as type-2 (CSNB2), depending on severity. In the complete form (CSNB1), there is no measurable rod cell response to light, whereas this response is measurable in the incomplete form. |
Statements
CID11:ID_587494652
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dki-india-ID_587494652
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Concluído
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15 August 2026
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