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Hyperoxaluria can be primary (as a result of a genetic defect) or secondary to another disease process. [citation needed] Type I primary hyperoxaluria (PH1) is associated mutations in the gene encoding AGXT, a key enzyme involved in oxalate metabolism. PH1 is an example of a protein mistargeting disease, wherein AGXT shows a trafficking defect.
Parasitic bronchitis, also known as hoose, husk, or verminous bronchitis, [1] is a disease of sheep, cattle, goats, [2] and swine caused by the presence of various species of parasite, commonly known as lungworms, [3] in the bronchial tubes or in the lungs. It is marked by cough, dyspnea, anorexia and constipation.
Brucellosis is a sexually transmitted bacterial disease that can cause uveitis, abortion, and orchitis in dogs. [6] Leptospirosis is an infectious disease caused by a spirochaete. Symptoms include liver and kidney failure and vasculitis. [10] Lyme disease* is a disease caused by Borrelia burgdorferi, a spirochaete, and spread by ticks of the ...
GBED is caused by an autosomal recessive mutation to the GBE1 gene, which leads glycogen branching enzyme activity that is reduced to absent. [1] Subsequently, glycogen molecules are produced with few branches, which greatly decreasing the number of nonreducing ends, drastically slowing the rate at which the molecule can be synthesized or ...
List of aquarium diseases; List of dog diseases; List of feline diseases; List of diseases of the honey bee; List of diseases spread by invertebrates; Poultry disease; Lists of zoonotic diseases, infectious diseases that have jumped from an animal to a human
It is the result of a mutation in the GBE1 gene, which causes a defect in the glycogen branching enzyme. Therefore, glycogen is not made properly, and abnormal glycogen molecules accumulate in cells; most severely in cardiac and muscle cells. The severity of this disease varies on the amount of enzyme produced.
Glycogen storage disease type V (GSD5, GSD-V), [1] also known as McArdle's disease, [2] is a metabolic disorder, one of the metabolic myopathies, more specifically a muscle glycogen storage disease, caused by a deficiency of myophosphorylase. [3] [4] Its incidence is reported as one in 100,000, roughly the same as glycogen storage disease type ...
A–I species cause disease in other animals, [19] ... core of the virion and is an enzyme called guanylyl ... due to lactase deficiency is a symptom of ...