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Navicular syndrome, often called navicular disease, is a syndrome of lameness problems in horses. It most commonly describes an inflammation or degeneration of the navicular bone and its surrounding tissues, usually on the front feet.
Horses just starting training may be lame due to a developmental orthopedic disease, such as osteochondrosis. Older animals are more likely to experience osteoarthritis. [10] Breed: Breed-specific diseases, such as hyperkalemic periodic paralysis (HYPP), can be ruled out. Additionally, some breeds or types are more prone to certain types of ...
Treatment and prognosis depend on the phase of the disease, with horses treated in earlier stages often having a better prognosis. Developmental phase. The developmental phase is defined as the time between the initial exposure to the causative agent or incident, until the onset of clinical signs.
Lameness is most commonly associated with injury to synovial joints, or those joints containing articular cartilage, a joint capsule, and a synovial membrane.Joint disease may affect the joint capsule and synovial membrane, articular cartilage, subchondral bone (the bone underneath the cartilage), menisci, or any ligaments associated with the joint.
Bone spavin indicated by A.. Bone spavin is osteoarthritis, or the final phase of degenerative joint disease (DJD), in the lower three hock joints.It usually affects the two lowest joints of the hock (the tarsometatarsal and the distal intertarsal joints), with the third joint, the proximal intertarsal, being the least likely to develop bone spavin.
The concussion comes from the rigorous training regimen that two-year-olds often face and inability of the bone to adapt fast enough. 70% of young Thoroughbred racehorses in training develop the problem, usually in the first six months. As horses become older, the cannon bone becomes stiffer and thus bucked shins rarely occur again.
Syndromes in horses (6 P) Pages in category "Horse diseases" The following 107 pages are in this category, out of 107 total. This list may not reflect recent changes.
The disease has a similar cause to Hirschsprung's disease in humans. A mutation in the middle of the endothelin receptor type B ( EDNRB ) gene causes lethal white syndrome when homozygous . Carriers, which are heterozygous —that is, have one copy of the mutated allele , but themselves are healthy—can now be reliably identified with a DNA test .