Labrador Retriever Health Panel 1

Description

Three Labrador Retrievers

This panel bundles together several genetic tests relevant to Labrador Retriever health.

Panel can be purchased on MyVGL. See below for pricing and list of specific tests included in panel.

Price

$165 per animal

Turnaround time

At least 15 business days; may be delayed beyond 15 business days if sample requires additional testing, or a new sample is requested.

Tests in This Panel

Centronuclear Myopathy (CNM) in Labrador Retrievers

Centronuclear myopathy is a hereditary myopathy of Labrador Retrievers characterized by generalized loss of muscle tone and control.

Congenital Myasthenic Syndrome (CMS) in Labrador Retrievers

Congenital myasthenic syndrome (CMS) is a neuromuscular disorder in Labrador Retrievers characterized by generalized muscle weakness and fatigue, often induced by exercise.

Copper Toxicosis (Menkes and Wilson diseases)

Copper toxicosis is a metabolic disorder that can cause chronic liver failure and neurological problems that result from deviations in normal levels of copper in the body.

Cystinuria Type I-A in Labrador Retrievers

Cystinuria type I-A is a kidney disorder in which the kidneys are unable to reabsorb cystine, leading to the formation of crystals in the urinary tract, which can cause urinary obstruction, difficulty in passing urine, and presence of blood in the urine.

Degenerative Myelopathy (DM)

Degenerative myelopathy (DM) is an inherited neurologic disorder of dogs characterized by gradual muscle wasting and loss of coordination typically beginning in the hind limbs. Testing is most appropriate for those breeds in which the clinical disease has been associated with the SOD1 allele.

Exercise-Induced Collapse (EIC)

Exercise-induced collapse is a genetic neuromuscular disorder characterized by muscle weakness, lack of coordination, and life-threatening collapse after intense exercise in otherwise apparently healthy dogs.

Hereditary Nasal Parakeratosis (HNPK)

Hereditary nasal parakeratosis is an inherited, recessive genetic defect that affects specialized cells of the canine nose, resulting in the formation of a crust with cracks over the nasal area of young dogs.

Hyperuricosuria (HUU)

Hyperuricosuria is an inherited disorder characterized by elevated levels of uric acid in the urine that can lead to the formation of bladder/kidney stones.

Narcolepsy in Labrador Retrievers

Narcolepsy in Labrador Retrievers is a sleeping disorder characterized by daytime sleepiness, fragmented sleep patterns, and sudden transient episodes of muscle weakness or paralysis triggered by play or food. This test detects a causal variant specific to Labrador Retrievers.

Pyruvate Kinase Deficiency (PKDef) in Labrador Retrievers

Pyruvate kinase deficiency in Labrador Retrievers is a chronic, severe hemolytic anemia caused by defective production of the enzyme pyruvate kinase. Signs in affected dogs may include lethargy, low exercise tolerance, and fatigue.

Progressive Rod-Cone Degeneration (PRA-prcd)

Progressive rod-cone degeneration (PRCD) is an inherited form of late-onset progressive retinal atrophy (PRA) that has been identified in many dog breeds.

Skeletal Dysplasia 2 (SD2) in Labrador Retrievers

Skeletal dysplasia 2 (SD2) is an inherited disorder that causes a mild form of disproportionate dwarfism consisting of short legs with normal body length and width.

Stargardt Disease in Labrador Retrievers

Stargardt disease is a degenerative eye disorder resulting from the progressive loss of the photoreceptor cells that are responsible for sensing light. Affected dogs show a decline in vision with age but appear to retain some vision throughout their life.

X-Linked Myotubular Myopathy (XLMTM) in Labrador Retrievers

X-linked myotubular myopathy in Labrador Retrievers is an inherited muscle disease that manifests with generalized muscle weakness and progressive muscle atrophy in puppies.

Type of Sample

Interdental/GUM brushes supplied by owner

Cytology Brush-supplied by VGL at no additional charge