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Congenital Stationary Night Blindness (CSNB) is an eye disorder that affects the retina, resulting in a total loss of low-light vision.
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Caractéristiques
| Breeds | |
|---|---|
| Gene | |
| Chromosome | 32 |
| Mutation | c.762_763delG |
| Mode of Inheritance | Autosomique récessif |
| Organ | |
| Specimen | Écouvillonnage, sanguin EDTA, sanguine hépariné, sperme, tissu |
| Also known as | CSNB |
Informations générales
Congenital Stationary Night Blindness (CSNB) is an eye disorder that affects the retina, resulting in a total loss of low-light vision. The disorder is caused by a recessive mutation to the gene LRIT3, and occurs in the Beagle.
Caractéristiques cliniques
Affected dogs are night blind; they have normal vision in bright-light conditions, but have great difficulty in seeing and navigating in dim light and in darkness. The disease is not expected to progress and worsen.
Additional Information
Références
Pubmed ID: 31578364
Year published: 2019
Omia ID: 1486
Omia variant ID: 1260