Color dilution and neurological defects (CDN)

General description

In the breed Miniature Dachshund, a variant in the gene MYO5A gene has been found to cause Coat Colour Dilution and Neurological Defects (CDN) resembling the human Griscelli Syndrome Type I.

Breeds

Dachshund (Dackel)

Order details
Test number8758
AbbreviationCDN
Sample material0.5 ml EDTA blood, 2x cheek swab, 1x special swab (eNAT)
Test duration7-14 working days
Test specifications
Symptom complexsystemic
Inheritanceautosomal recessive
Age of onset4 weeks
Causalitycausally
GeneMYO5A
MutationINS
LiteratureOMIA:001501-9615
Detailed description

In the breed Miniature Dachshund, a variant in the gene MYO5A gene has been found to cause Coat Colour Dilution and Neurological Defects (CDN) resembling the human Griscelli Syndrome Type I.\nAn affected 4-weeks old puppy showed a diluted, light red coat colour. Despite normally developed external features, the puppy was unable to hold a normal prone position, fell on its side and rowed with the upper front legs. Furthermore, it was unable to maintain an upright head position or to coordinate head movements and hardly reacted to environmental stimuli. The histopathological findings were a multifocal accumulation of melanin and a deposition of clumped keratin in the follicular epithelium of haired skin. Due to the severity of symptoms, the puppy was euthanized. A frameshift mutation in the MYO5A gene could be identified, myosin VA- mediated transport plays a crucial role in neurons and the cerebellum and also in melanosome transport into growing hair shafts.\n


Ihr Experte für Tiergenetik!

Yhteydenottopyyntö

LABOGEN on osa
LABOKLIN GMBH CO.KG
Kliinisen diagnostiikan laboratoriota

… jossa kokemus ja laatu kohtaavat!

Copyright © 2024 LABOGEN by LABOKLIN. All Rights Reserved.