Search results for: 'WA 0812 2782 5310 RAB Pemasangan Interior Rumah 30 Juta 2 Lantai WIlayah Sentolo Kulon Progo'

This panel includes the specific tests to be performed for Coton de Tuléar: neonatal ataxia (DOG-BNAT), canine multifocal retinopathy 2 (DOG-CMR2), Primary hyperoxaluria (DOG-OXA) and Von Willebrand disease type 1 (DOG-VWD1).

In domestic cats the common blood types are A and B, a third rare blood type AB is also known. This name is confusing as type AB is not the result of the presence of blood types A and B. A genetic mutation associated with blood group B in most cats has been identified. The genetic test can therefore determine whether a cat is bb (blood type B), Ab (blood type A or AB and carrier of the b allele) or AA (blood type A or AB). This test is particularly important in cats because of neonatal isoerythrolysis. The colostrum of a mother with blood group B can kill the kitten if it is of blood group A or AB.

Please note: this test is not valid for Ragdoll, Turkish Angora, and Neva Masquerade breeds. A specific test is available for each of these breeds.

This panel includes the specific tests to be carried out for American Staffordshire Terriers: cataract (DOG-HSF4-T), L2-hydroxyglutaric aciduria (DOG-L-2-HGA), Cerebellar Ataxia (DOG-NCLA) and Cone rod dystrophy 1 (DOG-PRA-CRD1).

Centronuclear myopathy is a condition characterised by a generalised loss of tone, muscle control, exercise intolerance and clumsy gait. This myopathy usually manifests itself in puppies at the age of 2-5 months.

This package includes the mandatory tests defined by the Flemish breeding program for French Bulldog: progressive retinal atrophy 4 (DOG-PRA-CRD4), canine multifocal retinopathy 1 (DOG-CMR1) and degenerative myelopathy 2 (DOG-DM2).

This pack includes the recommended tests defined by the Flemish breeding program for Staffordshire Bull Terrier: Progressive retinal atrophy 4 (CORD1) (DOG-PRA-CRD4), Degenerative myelopathy 2 (DOG-DM2) and Cataract (DOG-HSF4-T).

This panel includes the specific tests to be performed for the German Shorthaired Pointer: Acral Mutilation Syndrome (DOG-AMS), Exfoliative cutaneous lupus erythematosus (DOG-ECLE-GSHP), Junctional epidermolysis bullosa (DOG-JEB) and Von Willebrand disease type 2 (DOG-VWD2).

This package includes the mandatory tests defined by the Flemish breeding program for Airedale terrier:

Progressive retinal atrophy (DOG-PRA-CRD4), Degenerative myelopathy type 2 (DOG-DM2) and Fatal neonatal interstitial lung disease (DOG-LUNG).

Progressive Retinal Atrophy (PRA) is a genetic disease observed in dogs, particularly in the Swedish Vallhund breed. This disease is characterized by the multifocal appearance of red and brown discoloration in the ocular fundus, followed over time by thinning of the retina. It progresses in three stages: in Stage 2, there is a gradual loss of function of both rod and cone photoreceptors, measured by electroretinography. Night blindness occurs first at the end of Stage 2, followed by decreased daytime vision in Stage 3. Histological examinations confirm the loss of photoreceptor cells at Stage 3.

This test is also recommended for the Chinese Crested Dog as part of the breeding program established by the Flemish government (see official program).

This package includes the mandatory tests defined by the Flemish breeding program for Mastiff: multifocal retinopathy type 1 (DOG-CMR1) and Degenerative myelopathy 2 (DOG-DM2). The Flemish breeding program also recommends the tests included in our package DOG-MAST-VL+.