Search results for: 'WA 0852 2611 9277 Interior Rumah Minimalis 2 Lantai Lebar 5 Meter Cengkareng Jakarta Barat'

L-2-hydroxyglutaric aciduria is a genetic disease of the nervous system. The clinical signs are high levels of L-2-hydroxyglutaric acid in urine and plasma, seizures, wobbly gait, ataxia, tremors and muscle stiffness and usually appear from 6 months of age.

Neuronal ceroid lipofuscinoses (NCLs) are a group of lysosomal storage diseases that affect the central nervous system, leading to early neuronal death and progressive neurodegeneration. NCL2 specifically affects dachshunds, with symptoms including vision loss, tremors, and coordination problems starting at a young age. Unfortunately, there is no known cure for NCL2, and affected dogs typically do not survive past 12 months of age.

Cystinuria is a disorder that interferes with the proper reabsorption of cystine (an amino acid) in the kidneys leading to the formation of cystine crystals in the urine. Affected dogs have cystine crystals in the kidneys and/or bladder. 

Progressive retinal atrophy is an inherited eye disease characterized by bilateral degeneration of the photoreceptor cells of the retina resulting in progressive vision loss leading to total blindness. Other mutations can cause progressive retinal atrophy. 

Von Willebrand disease is a condition that causes excessive bleeding due to a lack or reduced level of von Willebrand factor (vWF), a blood clotting protein. 

Von Willebrand disease is a condition that causes excessive bleeding due to a deficiency or reduced levels of von Willebrand factor (vWF), a blood clotting protein.

This mutation is found in the Chinese Crested dog, but homozygous dogs do not appear to show clinical signs of bleeding disorders.

This pack includes the recommended tests defined by the Flemish breeding program for Golden Retriever: neuronal ceroid lipofuscinosis type 5 (DOG-NCL5GR), degenerative myelopathy type 2 (DOG-DM2), and ichthyosis type 2 (DOG-ICHGR-2).

The Flemish breeding program also requires the tests included in our DOG-RETRIVER-VL pack.

Hypocatalasia (or acatalasemia) is a rare genetic disorder caused by a mutation in the CAT gene, leading to a severe deficiency of catalase. This enzyme normally protects tissues against oxidative stress. The c.979G>A (p.Ala327Thr) mutation was first identified in a Beagle colony and subsequently detected in pet Beagles. A homozygous dog notably developed oral cavity gangrene with tooth loss at a young age. The disease may remain clinically silent for a long time, which highlights the importance of genetic screening in breeding dogs.
This test is also recommended for the Basset Hound as part of the Flemish government breeding program (see the official program).

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 test is also recommended for Labradoodle 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 Australian cattle dog: Degenerative myelopathy 2 (DOG-DM2), Neuronal ceroid lipofuscinosis type 12 (DOG-NCL12-ACD), Neuronal ceroid lipofuscinosis type 5 (DOG-NCL5), Primary lens luxation (DOG-PLL), Progressive rod-cone degeneration (DOG-PRA-PRCD). The Flemish breeding program also recommends the tests included in our package DOG-AC-VL+.