0,- 0,- hors TVA

Only available in bundles

H422

Protein Losing Nephropathy (PLN) is a condition in which the kidneys lose significant amounts of protein, particularly albumin, into the urine.

10 working days

Excl €5,95 shipping and administration per order (incl. VAT)

Only available in bundles

Caractéristiques

Breeds

,

Gene

Organ

specimen

Écouvillonnage, sanguin EDTA, sanguine hépariné, sperme, tissu

Mode of Inheritance

Chromosome

Also known as

Year Published

Informations générales

Protein Losing Nephropathy (PLN) is a condition in which the kidneys lose significant amounts of protein, particularly albumin, into the urine. This happens when the kidney’s filtration system (specifically the glomeruli) becomes damaged, allowing proteins that should be retained in the blood to pass into the urine. This leads to muscle wasting, abnormal fluid accumulation in the skin and limbs, and kidney failure.

Dogs carrying one or two copies of this mutation are at risk for developing PLN, with those possessing two copies having a significantly higher likelihood of the disease. However, this mutation is incompletely penetrant, indicating that other genetic and environmental factors also play a role in the disease’s development.

Risk assessment for PLN in the Soft Coated Wheaten Terrier and Airedale Terrier can be done by screening for two different mutations (one on gene KIRREL2 and one on gene NPHS1) that both code for proteins that determine the size of the molecules that can be filtrated by the kidneys. The mutation tested here is KIRRELL2.

Caractéristiques cliniques

In dogs, PLN can lead to a variety of symptoms, primarily related to the loss of protein and its effects on body functions. Symptoms may include fluid accumulation in the abdomen, skin, and limbs, and, ultimately, kidney failure. Also weight loss, weakness and lethargy, decreased appetite, vomiting or diarrhea, dehydration and increased (foamy) urine can be observed.

Additional Information

Dogs homozygous for the PLN-predisposing haplotype, and thus have the amino acid substitutions in both NPHS1 and KIRREL2, are at very high increased risk of developing PLN compared to dogs that are heterozygous or homozygous for the ‘‘normal’’ haplotype or alleles.

Références

Pubmed ID: 23325127

Omia ID: 1326

Comment ça marche?

1. Sélectionnez vos produits

Sélectionnez un seul test, un package CombiBreed ou créez votre propre package.

2. Prélevez un échantillon d’ADN

Prélevez le matériel d’ADN comme indiqué avec nos produits et envoyez-le au laboratoire.

3. Résultat

Nous traitons votre commande avec soin et vous communiquons les résultats.