€57,48 €47,50 IVA no incluido
Congenital Stationary Night Blindness 2 (CSNB2) is a genetic retinal disorder characterized by impaired vision in low light conditions.
10 días laborables
Especificaciones
| Breeds | American Trotter, Caballo de las Montañas Rocosas, Caballo de miniatura, Caballo de Tennessee, Cuarto de caballo americano, Saddlebred americano, Trotter zorro de Missouri, Morgan |
|---|---|
| Gene | |
| Chromosome | 14 |
| Mutation | c.533C>T |
| Mode of Inheritance | Autosómico recesivo |
| Organ | |
| Specimen | Pelo, sangre EDTA, sangre Heparina, Semen, Tejido |
| Also known as | CSNB2 |
Información específica de la prueba
Congenital Stationary Night Blindness 2 (CSNB2) is a genetic retinal disorder characterized by impaired vision in low light conditions. It is caused by an autosomal recessive mutation in the metabotropic glutamate receptor 6 (GRM6) gene, which is essential for transmitting visual signals from rod photoreceptors to ON-bipolar cells in the retina. The mutation disrupts signal transmission in dim light, resulting in night blindness despite a structurally normal eye.
This disorder is distinct from the Leopard Complex (LP)/Appaloosa-associated form of night blindness and was first identified in a Tennessee Walking Horse. The variant has since been reported in additional breeds.
Características clínicas
Affected horses have normal vision in daylight but show difficulty seeing in low-light or dark conditions. Clinical signs are typically present from birth, although they may become more noticeable as young horses begin navigating unfamiliar environments. Horses may hesitate to move in poorly lit areas, appear anxious when entering dark spaces, struggle to detect obstacles at dusk or night, and may be at increased risk of accidental injury in low-light conditions.
CSNB2 is non-progressive and does not worsen over time. It does not affect overall health or lifespan, but it may impact management and safety in environments with limited lighting.
Información adicional
Referencias
Pubmed ID: 32654228
Year published: 2021
Omia ID: 2692
Omia variant ID: 1552