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This package includes the mandatory tests defined by the Flemish breeding program for American Staffordshire Terrier: degenerative myelopathy type 2 (DOG-DM2), neuronal ceroid lipofuscinosis 4A (DOG-NCLA), progressive retinal atrophy type 4 (DOG-PRA-CRD4) and progressive retinal atrophy type 1 (DOG-PRA-RCD1).

The Flemish breeding program also recommends the tests included in our DOG-AMSTAFF-VL+ pack.

Hypomyelination, also known as Shaking pup syndrome, is a disorder of the nervous system caused by a defect in the myelination of the spinal cord. Affected dogs show tremors, walking difficulties, balance and coordination problems. This disease is transmitted in an X-linked recessive manner, so males carrying the mutation will all be affected. However, only females with 2 copies of the mutated allele will be affected.

This package includes the mandatory tests defined by the Flemish breeding program for Labradoodle: Degenerative myelopathy 2 (DOG-DM2), Centronuclear myopathy (DOG-CNM), Exercise-induced collapse (DOG-EIC), Hereditary nasal parakeratosis (DOG-HNPK), Progressive rod-cone degeneration (DOG-PRA-PRCD), Stargardt disease (DOG-STGD) and Von Willebrand disease type 1 (DOG-VWD1). The Flemish breeding program also recommends the tests included in our package DOG-DOODLE-VL+.

This pack includes the recommended tests defined by the Flemish breeding program for German Shorthaired Pointer: Achromatopsia (CNGB3) (DOG-ACHM3), Acral Mutilation Syndrome (DOG-AMS), ichtyosis type 1 (DOG-ICHGR-1), Progressive rod-cone degeneration (DOG-PRA-PRCD), Stargardt disease (DOG-STGD) and Von Willebrand disease type 2 (DOG-VWD2-BA). The Flemish breeding program also makes the tests included in our package mandatory DOG-BRQALLD-VL.

The locus D or dilution refers to a mutation in the MLPH gene that causes a diluted coat colour. This mutation dilutes black to blue, chocolate to lilac and yellow to champagne. The mutation tested is the d^2 mutation and is specific to the Chow Chow, Sloughi and Thai Ridgeback breeds. For the other breeds, the test to be performed is the DOG-LOCUS-D test.

Familial nephropathy (FN) is a genetic disease affecting the kidneys. Dogs with this disorder develop progressive kidney failure leading to death. The first symptoms usually appear between 6 months and 2 years of age and include excessive water consumption, weight loss, decreased appetite, diarrhea and vomiting.

This test is also recommended for English Springer Spaniel as part of the breeding program established by the Flemish government (see official program).

Lethal acrodermatitis is a genetic disease of the immune system. The clinical signs are skin lesions on the paws and muzzle, leading to secondary infections. In addition, the lesions cause hyperkeratosis of the pads and deformation of the nails. Affected puppies also suffer from diarrhea, bronchopneumonia and retarded growth. The first symptoms appear quickly after birth. Affected puppies usually die before 2 years of age or are euthanized.

Golden Retriever muscular dystrophy is a homologue of Duchenne muscular dystrophy in humans. Affected dogs develop clinical signs at 8 to 10 weeks of age. Symptoms include a shuffling gait, inability to fully open the jaw, difficulty eating, curvature of the spine and ribs, resulting in a squatted posture. he disease is transmitted in an X-linked recessive manner, so males carrying the mutation will all be affected. However, only females with 2 copies of the mutated allele will be affected.

This package includes the mandatory tests defined by the Flemish breeding program for Miniature American Shepherd: Collie eye anomaly (DOG-CEA), Cataract (DOG-HSF4-BA), Multidrug Resistance 1 (DOG-MDR1), Degenerative myelopathy 2 (DOG-DM2), Coat color merle (DOG-LOCUS-M), Progressive rod-cone degeneration (DOG-PRA-PRCD), Progressive retinal atrophy (DOG-PRA-BBS2), Neuroaxonal dystrophy (DOG-NAD-MAS) and Progressive retinal atrophy 4 (CORD1) (DOG-PRA-CRD4). The Flemish breeding program also recommends the tests included in our package DOG-BGAM-VL+.

Neuro-axonal dystrophy (NAD) in Papillon dogs is a rare inherited neurological disorder that causes progressive degeneration of the central nervous system.
Signs appear very early, usually between 2 and 4 months of age, and include gait abnormalities, head and limb tremors, weakness of the hind limbs, and in some cases, involvement of the forelimbs or visual deficits.
The progression is rapid and severe: affected dogs may have difficulty eating and are often euthanized shortly after the onset of symptoms due to a reserved vital prognosis.