Congenital stationary night blindness (Q99765): Difference between revisions
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Trata-se de um raro transtorno retiniano não progressivo ligado ao X. Possui duas formas dependendo da gravidade: completa, também conhecida como tipo 1 (CSNB1), e incompleta, também conhecida como tipo 2 (CSNB2). Na forma completa (CSNB1), não há resposta à luz mensurável em cones, enquanto há resposta mensurável na forma incompleta | |||
| description / en | description / en | ||
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. | |||
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. |
