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Canine follicular dysplasia. Follicular dysplasia is a genetic disease of dogs causing alopecia, also called hair loss. It is caused by hair follicles that are misfunctioning due to structural abnormality. There are several types, some affecting only certain breeds. Diagnosis is achieved through a biopsy, and treatment is rarely successful.
Canine discoid lupus erythematosus showing loss of noseprint, depigmentation, ulceration and tissue destruction - all characteristic of the syndrome. The most common initial symptom is scaling and loss of pigment on the nose. The surface of the nose becomes smooth gray, and ulcerated, instead of the normal black cobblestone texture.
Atopy is a hereditary [ 3] and chronic (lifelong) allergic skin disease. Signs usually begin between 6 months and 3 years of age, with some breeds of dog, such as the golden retriever, showing signs at an earlier age. Dogs with atopic dermatitis are itchy, especially around the eyes, muzzle, ears and feet. In severe cases, the irritation is ...
Waardenburg syndrome is a group of rare genetic conditions characterised by at least some degree of congenital hearing loss and pigmentation deficiencies, which can include bright blue eyes (or one blue eye and one brown eye ), a white forelock or patches of light skin. These basic features constitute type 2 of the condition; in type 1, there ...
Sebaceous adenitis and hair loss in a dog. Sebaceous adenitis in an uncommon skin disease found in some breeds of dog, and more rarely in cats, rabbits and horses. [1] characterised by an inflammatory response against the dog's sebaceous glands (glands found in the hair follicles in the skin dermis), which can lead to the destruction of the gland.
They have relaxed body language. “Happy dogs should have very loose body language,” Anderson said. “They shouldn’t have any tension. Their ears shouldn’t be pulled back. You shouldn’t ...
Progressive retinal atrophy (PRA) is a group of genetic diseases seen in certain breeds of dogs and, more rarely, cats. Similar to retinitis pigmentosa in humans, [ 1] it is characterized by the bilateral degeneration of the retina, causing progressive vision loss culminating in blindness. The condition in nearly all breeds is inherited as an ...
Hyperkeratosis is thickening of the stratum corneum (the outermost layer of the epidermis, or skin ), often associated with the presence of an abnormal quantity of keratin, [ 1] and is usually accompanied by an increase in the granular layer. As the corneum layer normally varies greatly in thickness in different sites, some experience is needed ...
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