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Up to 80 percent of dogs infected will have symptoms, but the mortality rate is only 5 to 8 percent. [5] Infectious canine hepatitis is a sometimes fatal infectious disease of the liver. [6] Canine herpesvirus is an infectious disease that is a common cause of death in puppies less than three weeks old. [7]
Hypertrichosis (better known as Werewolf Syndrome) is an abnormal amount of hair growth over the body. [1] [2] The two distinct types of hypertrichosis are generalized hypertrichosis, which occurs over the entire body, and localized hypertrichosis, which is restricted to a certain area. [1]
In the United States, R. sanguineus is a vector of many disease-causing pathogens in dogs, including Ehrlichia canis, which causes canine ehrlichiosis, and Babesia canis, which is responsible for canine babesiosis. In dogs, symptoms of canine ehrlichiosis include lameness and fever; those for babesiosis include fever, anorexia, and anemia.
Immune-mediated hemolytic anemia is a devastating disease that causes severe anemia in dogs through red blood cell destruction by the immune system. It has been associated with vaccinations and certain drugs, although many cases are idiopathic .
Babesia canis is a parasite that infects red blood cells and can lead to anemia. [1] This is a species that falls under the overarching genus Babesia.It is transmitted by the brown dog tick (Rhipicephalus sanguineus) and is one of the most common piroplasm infections. [2]
13-year-old Lalit Patidar from central India was given the nickname ''wolf boy'' after the effects of a rare condition, known as hypertrichosis, caused him to grow hair all over his face ...
People who have these mutations are also at an increased risk of developing porphyria cutanea tarda. [ citation needed ] In the 20% of cases where porphyria cutanea tarda is inherited, it is inherited in an autosomal dominant pattern, which means one copy of the altered gene is sufficient to decrease enzyme activity and cause the signs and ...
Cantú syndrome is a rare condition characterized by hypertrichosis, osteochondrodysplasia, and cardiomegaly. [ 6 ] [ 5 ] Fewer than 50 cases have been described in the literature; they are associated with a mutation in the ABCC9 -gene that codes for the ABCC9-protein.