kr667,40 kr551,57 ekskl. mva

H186

Startle disease in dogs, also known as hyperekplexia, is a rare neurological condition that causes affected dogs to have exaggerated, sudden responses to stimuli.

10 Arbeidsdager

Spesifikasjoner

Breeds

Gene

Organ

specimen

Svaber, EDTA blod, heparinblod, sæd, vev

Mode of Inheritance

Chromosome

Also known as

Year Published

Generell informasjon

Startle disease in dogs, also known as hyperekplexia, is a rare neurological condition that causes affected dogs to have exaggerated, sudden responses to stimuli. An autosomal recessive mutation that can lead to startle disease is found in the Solute Carrier Family 6 Member 5 (SLC6A5) gene. This gene encodes the glycine transporter 2 (GlyT2), which is responsible for the reuptake of glycine. When this reuptake is impaired the normal inhibitory signalling in the spinal cord and brainstem is disrupted. This leads to an extreme sensitivity to environmental stimuli and overactivation of motor neurons, causing the excessive startle responses and muscle rigidity characteristic of startle disease. The mutation in the SLC6A5 gene has been observed in the Old English Sheepdog.

Kliniske egenskaper

Dogs with startle disease exhibit extreme sensitivity to touch or noise, reacting strongly to everyday stimuli. After being startled, they may display stiffness, become rigid or frozen for short periods. Additionally, the neurological effects of the condition can cause difficulty with movement, leading to problems with walking or coordination.

Tilleggsinformasjon

Referanser

Pubmed ID: 40012122

Omia ID: 1594

Hvordan virker det?

1. Velg ønsket produkt(er).

Velg enkelttest, en kombinasjonspakke eller lag din egen pakke

2. Innhent DNA-prøve

Samle materiale til DNA-testen som vist på bruksanvisning for din testtype og send prøven til laboratoriet

3. Resultat

Vi utfører analysen på din prøve og sender deg testsvaret