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Topic:Polysaccharide Storage Myopathy
Polysaccharide Storage Myopathy (PSSM) is a hereditary muscle disorder affecting horses, characterized by the abnormal accumulation of glycogen and polysaccharides in skeletal muscle tissue. This condition can lead to muscle stiffness, weakness, and pain, particularly after exercise. PSSM is primarily associated with specific genetic mutations that affect glycogen synthesis and storage. Horses with PSSM may exhibit symptoms such as reluctance to move, sweating, and muscle tremors. Diagnosis typically involves muscle biopsy and genetic testing. This page compiles peer-reviewed research studies and scholarly articles that explore the genetic basis, pathophysiology, and management strategies for Polysaccharide Storage Myopathy in equine populations.
Diagnosis and treatment of the navicular syndrome in horses. Navicular syndrome can be treated in a variety of ways. This is related to the fact that it has a variety of causes. Prognostically, most horses will improve with treatment. One can expect about 50 per cent of the horses to become useably sound for 1 year, no matter what treatment is used. The disease is progressive, and affected horses eventually will need to be retired because of lameness. The author's therapeutic approach is to utilize shoeing as the primary therapy. Shoeing is performed to correct structural problems and to ensure that shoeing is physiologically sound. Nonsteroidal anti-in...
Review of pathogenesis and treatment of degenerative joint disease. Treatment of degenerative joint disease (osteoarthritis) is discussed in relationship to pathogenesis of five clinical entities, defined to facilitate discussion:-1) occurring in high motion joints and associated with synovitis; 2) associated with low motion joints; 3) "non-progressive" articular cartilage erosion; 4) secondary to other identified problems (intra-articular fractures, ligamentous damage, wounds, septic arthritis, osteochondrosis); and 5) chondromalacia of the patella. In addition to direct damage to articular cartilage, synovitis and capsulitis and depletion of matrical glycosa...
Polysaccharide storage myopathy. In a woman with a slowly progressive adult onset proximal myopathy, muscle biopsy showed storage of PAS positive material in type 1 fibers. This material consisted of a branched chain polysaccharide associated with a mucoprotein. No abnormality of glycogen-pathway enzymes was detected. This suggested that this polysaccharide accumulation occurred because the polysaccharide was laid down in a non-bioavailable form. The clinical and histochemical features in this patient and in the few similar reported cases indicate that polysaccharide storage myopathy is a distinct entity that is allied to the...
Immunochemistry of pneumococcal types II, V, and VI. II. Inhibition tests in the type VI precipitating system. Rebers, Paul A. (Rutgers University, New Brunswick, N. J.), Esther Hurwitz, and Michael Heidelberger. Immunochemistry of pneumococcal types II, V, and VI. II. Inhibition tests in the type VI precipitating system. J. Bacteriol. 82:920-926. 1961.-As in other immune systems involving polysaccharides, rabbit antibodies but not those engendered in the horse were found sensitive to degradation of type VI pneumococcal (Pn) polysaccharide (SVI), and were readily inhibited by fragments of SVI. Large amounts, 30 to 111 mumoles, of most sugars gave up to 15% inhibition, while sugar and polyol phosphates ...
Polysaccharide storage myopathy in an Australian Quarter Horse. The study investigates the case of an Australian Quarter Horse suffering from Polysaccharide Storage Myopathy (PSSM), a muscular disease commonly seen in Quarter Horse breeds, Warmbloods, and draft horses. This […]
Epidemiological and genetic study of exertional rhabdomyolysis in a Warmblood horse family in Switzerland. Exertional rhabdomyolysis (ER) and its familial basis in Warmblood horses is incompletely understood. Objective: To describe the case details, clinical signs and management of ER-affected Warmblood horses from a family with a high prevalence of ER, to determine if histopathological signs of polysaccharide storage myopathy (PSSM) and the glycogen synthase (GYS1) mutation are associated with ER in this family, and to investigate potential risk factors for development of ER. Methods: A family consisting of a sire with ER and 71 of his descendants was investigated. History of episodes of ER, husba...
Polysaccharide storage myopathy in the M. longissimus lumborum of showjumpers and dressage horses with back pain. This study was designed to investigate whether horses with clinical signs of back pain due to suspected soft tissue injuries were affected by polysaccharide storage myopathy (PSSM). Diagnosis of PSSM in muscle biopsies obtained from the M. longissimus lumborum of 5 showjumpers and 4 dressage horses with a history of back pain is reported. M. longissimus lumborum biopsies of these horses were characterised histopathologically and in 3/9 cases also by electron microscopy. Observations were compared with M. gluteus biopsies of the same horses, and with M. gluteus biopsies obtained from 6 Standard...
