Search results
Results from the WOW.Com Content Network
Fibrodysplasia ossificans progressiva (/ ˌ f aɪ b r oʊ d ɪ ˈ s p l eɪ ʒ (i) ə ɒ ˈ s ɪ f ɪ k æ n z p r ə ˈ ɡ r ɛ s ɪ v ə /; [1] abbr. FOP), also called Münchmeyer disease or formerly myositis ossificans progressiva, is an extremely rare connective tissue disease in which fibrous connective tissue such as muscle, tendons, and ligaments turn into bone tissue (ossification).
The disease was first reported in 1996. [4] The first cases were found in Fell ponies, and the disease was initially termed "Fell pony syndrome." [1] The disease appeared to have a genetic component, and, after hereditary diseases known to affect other horse breeds were investigated, it was concluded that this was a newly identified disease. [1]
The Belgian Draft Horse is one breed in which JEB occurs Junctional epidermolysis bullosa ( JEB ) is an inherited disorder that is also known as red foot disease or hairless foal syndrome . [ 1 ] JEB is the result of a genetic mutation that inhibits protein production that is essential for skin adhesion. [ 2 ]
The International Fibrodysplasia Ossificans Progressiva Association (IFOPA) is a US-based 501(c)(3) non-profit organization supporting medical research, education and communication for those afflicted by the rare genetic condition Fibrodysplasia Ossificans Progressiva (FOP). IFOPA's mission is to fund research to find a cure for FOP while ...
Equine encephalosis virus; Equine exertional rhabdomyolysis; Equine gastric ulcer syndrome; Equid alphaherpesvirus 1; Equid alphaherpesvirus 3; Equine infectious anemia; Equine influenza; Equine melanoma; Equine multinodular pulmonary fibrosis; Equine polysaccharide storage myopathy; Equine protozoal myeloencephalitis; Equine proximal enteritis ...
The same should be done when cooling down. Ensure that the horse is cared for, for an issues to the immune system and allowed to recover before continuing training. [1] A horse ideally should receive exercise once, or possibly twice a day, every day, to prevent the recurrence of ER. If possible, avoid breaks in the horse's exercise schedule. [1]
Horses heterozygous for the Ile118Lys mutation on the equine EDNRB gene—carriers of lethal white syndrome—usually exhibit a white-spotting pattern called "frame", or "frame overo". [ 5 ] [ 7 ] [ 9 ] [ 13 ] Frame is characterized by jagged, sharply defined, horizontally oriented white patches that run along the horse's neck, shoulder, flank ...
Equine polysaccharide storage myopathy (EPSM, PSSM, EPSSM) is a hereditary glycogen storage disease of horses that causes exertional rhabdomyolysis.It is currently known to affect the following breeds American Quarter Horses, American Paint Horses, Warmbloods, Cobs, Dales Ponies, Thoroughbreds, Arabians, New Forest ponies, and a large number of Heavy horse breeds.