Labradore vom Vorgebirge

A cataract is a progressive clouding of the lens inside the dog's eye, which is the clear structure that focuses light onto the retina at the back of the eye. When the lens becomes cloudy or opaque, it blocks light from entering, gradually impairing the dog's vision. If left untreated, this condition can eventually lead to complete blindness in the affected eye.

Progressive Retinal Atrophy (PRA) is an inherited eye disease that affects the retina, which is the light-sensitive layer of tissue at the back of the eye. In this condition, the specialized cells responsible for detecting light, known as photoreceptors, gradually degenerate and die. Because these cells cannot recover or be replaced, the disease slowly but inevitably leads to complete blindness.

Retinal dysplasia is a congenital condition affecting the eyes, where the retina (the light-sensitive tissue at the back of the eye) does not develop properly during growth in the womb. This abnormal development leads to structural defects like folds or gaps in the retinal layers. Because the retina is responsible for sending visual signals to the brain, these imperfections can impair normal vision.

Hereditary Nasal Parakeratosis (HNPK) is an inherited skin disorder that affects the nose. It is caused by a genetic defect that disrupts keratinization, which is the natural process where skin cells mature and form a protective, moisture-retaining outer layer. Without this barrier, the skin on the nose becomes extremely dry, thick, and prone to damage.

Elbow dysplasia is a developmental disorder of the musculoskeletal system where the three bones forming the elbow joint do not fit together properly. This misalignment causes abnormal friction and wear on the joint cartilage, eventually leading to painful, chronic joint inflammation and arthritis. It is a complex genetic condition influenced by multiple genes.

Exercise Induced Collapse (EIC) is an inherited disorder of the nervous system where the communication between the brain and the muscles temporarily breaks down during intense physical activity or high excitement. This neurological failure prevents the muscles from receiving the signals they need to function properly, causing a sudden loss of motor control. It is inherited in an autosomal-recessive manner, meaning a dog must inherit the mutated gene from both parents to be affected.

Hip dysplasia is an inherited skeletal disorder where the ball and socket of the hip joint do not fit together properly. Instead of sliding smoothly, the bones rub and grind against each other, wearing down the protective cartilage. Over time, this chronic friction causes joint instability, painful inflammation, and progressive arthritis, which is the gradual wear and tear of the joint.

This refers to a variety of hereditary eye conditions affecting the structures of the eye, such as the lens, retina, or eyelids. An ophthalmological eye exam is a specialized clinical screening used to detect these genetic defects, which include cataracts (clouding of the lens) or progressive retinal atrophy (gradual degeneration of the light-sensitive retina). Early detection through these screenings helps identify issues before they cause permanent vision loss or chronic pain.

These are structural eyelid abnormalities affecting a dog's eyes. In cases of entropion, the eyelid rolls inward, causing the eyelashes or fur to rub painfully against the surface of the eyeball. In ectropion, the eyelid sags or rolls outward, leaving the sensitive inner lining of the eye exposed and unprotected.

Central Progressive Retinal Atrophy (CPRA) is an inherited eye disease that affects the retina, which is the light-sensitive layer at the back of the dog's eye. In this condition, the supporting cells of the retina fail to properly process waste and transport nutrients to the light-sensing cells. Over time, this metabolic failure causes these light-sensing cells to slowly deteriorate, resulting in a gradual loss of vision.

Epilepsy is a chronic disorder of the brain and nervous system where abnormal electrical activity causes sudden, temporary disruptions in normal brain function. These disruptions lead to repeated seizures, which are involuntary changes in body movement, sensation, or behavior. Because the underlying cause is often complex, the brain's electrical signaling remains permanently prone to these sudden misfires.

This is an inherited muscle disease affecting the skeletal muscles of dogs. It is caused by a genetic defect that prevents muscle fibers from developing normally, leading to progressive muscle wasting where the muscles gradually shrink and weaken.

Skeletal Dysplasia 2 (SD2) is an inherited bone growth disorder affecting the skeletal system. It causes a mild form of disproportionate dwarfism, where the long bones of the legs do not grow to their normal length. The torso and head develop normally, resulting in a slightly uneven body shape.