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A dermoid sinus is a defect that occurs during embryonic development that results in an incomplete separation between the skin and the neural tube, the structure present during embryonic life which gives rise to the central nervous system (brain and spinal cord). A sinus (blind infected tract) forms that may extend from the skin to the dura mater (the outermost, toughest and most fibrous membrane that covers the brain and spinal cord) of the spinal cord or may end as a blind sac in the tissue below the skin.
It has the highest incidence in Rhodesian Ridgebacks, but has also been reported as congenital defects in Shih Tzu and boxer breeds.
The sinus has single or multiple small openings that may have tufts of hair protruding from them and may be found anywhere along the midline of the back, but is most common over the cervical (neck) spine. A cord may be clearly palpable. The sinus may contain sebum, keratin, debris and hair, and sinuses may even become inflamed, infected , and drain. Sinuses that extend to the the spinal cord may also lead to bacterial meningoencephalitis.
A diagnosis is usually based on the history, clinical signs and a fistulogram (radiograph of the tract after infusion of radiopaque material).
Draining tracts requires surgical removal of the sinus.
P The prognosis is good, but affected dogs should not be bred.
It is commonly known as black skin disease (BSD). The current term alopecia X is used to emphasize that the origin of this disorder is not yet known. The condition is found in Nordic breeds e.g. Pomeranian, Spitz and Samoyed, but is also described in Miniature Poodles. The strong breed predisposition and a pedigree analysis of affected individuals suggest a hereditary background. Although male and female dogs can be affected, males are more frequently affected. In most cases the age of onset is between 9 months and 2 years.
Hairless patches are seen at the root of the tail, at the back, at the limbs from the thigh to the tarsus and at the abdomen. Within the hairless patches, the skin is darkly pigmented and some islets with sparse hair may be present.
The diagnosis is made based on the history, clinical findings and exclusion of other possible causes such as hypothyroidism and hyperandrenocorticism..
The condition is mostly a cosmetic problem. Hair regrowth is expected after castration of male dogs, but recurrence after one year is possible. Melatonin has been reported to be effective, but Trilostane is regarded as the most effective and safe drug for the disease.
Entropion is the inversion of part or all of the eyelid margin, resulting in eyelashes making contact with the cornea. Hereditary is the most common cause of entropion and it occurs as a congenital defect in many breeds.
The overflow of tears, rolling in of the eyelid, inflammation of the conjunctiva as well as corneal ulceration may be present.
Neonatal entropion in puppies may be corrected by means of eyelid tacking. In puppies older than 3 months of age, surgical correction may be indicated.
A catacract is an opacity caused by the disruption of the normal arrangements of the lens fibres or lens capsule. Hereditary is the most common cause of cataracts in dogs, and it can be either congenital or develop up to 5 years of age. Other possible causes include diabetes mellitus, milk replacements, chemicals, radiation, electric shock, trauma, ageing.
Will vary depending on the maturation of the cataract(s) and may include no visual defects, varying degrees of vision and blindness.:
Removal of the lens and its capsule as an intact unit, removal of the anterior capsule and lens contents, or the ultrasonic fragmentation and aspiration of the lens.
Progressive retinal atrophy is also known as rod-cone degeneration and is the most common inherited cause of blindness in dogs. In most cases it is transmitted as an autosomal recessive disease, and different dog breeds have different forms of the disease. It has been reported as an inherited condition in the following breeds: American and English Cocker Spaniels; Miniature and toy poodles: Labrador Retrievers; Portuguese Water Dogs: Akita, Miniature Long Haired Dachshund; Papillon; Tibetan Terrier;; Tibetan Spaniel; Siberian Huskies; Miniature Schnauzer.
The age of onset varies. The initial behavioural sign is usually loss of night vision. the disease is progressive, invariably leading to blindness.
Congenital deafness can either be inherited, or result from damage to the developing foetus. Merle and white coat colours are associated with congenital deafness in dogs. Dog breeds that are commonly affected include the Dalmation, Australian Shepherd, Catahoula, English Setter, Australian Shepherd, Boston Terrier, Old English Sheepdog, Great Dane, West Highland White Terrier, and Boxer. The list of affected breeds currently consists of over 48 breeds and it continues to expand and may change due to breed popularity and elimination of the defect through selective breeding.
The primary signs of deafness is failure to respond to an auditory stimulus, but other signs include unusual behaviour such as excessive barking. In congenital deafness, examination of the external ear, radiographs and neurologic examination are normal, but the animal shows evidence of a lack of hearing.
For more information on other Congenital Defects in Dogs: Canine Leukocyte Adhesion Deficiency - CLAD Congenital Portosystemic - Shunts in dogs Return from Skin Eyes and Ears of dogs to Veterinary Articles
Veterinary articles supplied by Dr S Strydom and published with kind permission of DIA Publishing - publishers of KUSA Dogs in Africa Magazine Dr Sunelle Strydom qualified as a veterinarian in 2004 at the Faculty of Veterinary Science, University of Pretoria. She has a passion for writing and the sharing of knowledge to promote animal health and welfare. She has written several articles for KUSA Dogs in Africa as well as for Vra vir Faffa on the Landbouweekblad website at www.landbou.com
References
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