Pereiti prie pagrindinio turinio

Adresas

Panerių g. 246
48454 Kaunas
Lietuva

Darbo laikas

  • Pi – Pe
    9 :00 – 17 00
  • Še  
    Nedirbame    
  • Se
    Nedirbame   
Dog DNA testing illustration

Juvenile Cataract – Wirehaired Pointing Griffon

Kodas: H154

74,72 €

Mėginio duomenys

Vienas tyrimas – vienas mėginys. Gyvūno ir savininko duomenys neprivalomi.

Ieškokite pagal mūsų ar laboratorijos numerį. Nerastas numeris išsaugomas kaip ankstesnis / išorinis numeris. Naujo fizinio mėginio nereikia.
Įdėjimo į krepšelį mygtukas pasirodys po to, kai aukščiau pasirinksite reikšmę

Short description

Juvenile cataract is characterized by clouding of the eye’s lens, which impairs vision and can lead to total blindness if the condition progresses.

General information

Juvenile cataract is characterized by clouding of the eye’s lens, which impairs vision and can lead to total blindness if the condition progresses. The lens normally focuses light onto the retina, enabling clear vision. Cataract can develop due to aging, injury, underlying diseases or genetic defects and can occur in one eye or in both eyes. Cataracts are common in most dogs from around the age of seven onwards, to varying degrees, due to the natural aging process of the lens. This specific variant affects juvenile Wirehaired Pointing Griffons and is caused by an autosomal recessive mutation in the FYVE And Coiled-Coil Domain Autophagy Adaptor 1 (FYCO1) gene.

Specifications

Breeds

Wirehaired Pointing Griffon

Gene

FYCO1

Chromosome

20

Mutation

c.2024delG

Organ

Sensory organs

Specimen

Swab, Blood EDTA, Blood Heparin, Semen, Tissue

Mode of Inheritance

Autosomal Recessive

Clinical features

Affected dogs develop progressive lens opacities in both eyes that begin as cloudy spots in the lens and worsen over time. Clinical symptoms include clumsiness, imbalance, and difficulty navigating their environment. Progression lead to complete blindness, which has been observed already at 8 weeks of age in the original publication. However, it is unknown if progression is always this fast.

References

Pubmed ID: 35205377

Year published: 2022

Omia ID: 2536

Omia variant ID:

Turnaround information

  • 10 working days