According to the research, the correct option is Period of invasion. The stage of an infectious disease when specific signs and symptoms are seen and the pathogen is at peak activity is the Period of invasion.
<h3>What is an infectious disease?</h3>
It is the disease that is due to the invasion of the body by pathogenic germs, which establish and multiply caused by a local cell injury, secretion of toxins or by the antigen-antibody reaction.
The stage of an infectious disease called the Period of invasion is the time interval between invasion by an infectious agent and the appearance of the first signs and symptoms of the disease.
Therefore, we can conclude that according to the research, the correct option is Period of invasion. The stage of an infectious disease when specific signs and symptoms are seen and the pathogen is at peak activity is the Period of invasion.
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Answer:
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Explanation:
3.3 cm esta es la resouesta .
She should consult her physician and insurance company in charge of the plan in this scenario.
<h3>What is Insurance?</h3>
This is the means of protection from any form of loss or theft and comprises of different types such as medical etc.
The physician and insurance company will have to liaise with one another to prevent double payment by the client.
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Answer: Mutations in the GALT, GALK1, and GALE genes cause galactosemia.
Explanation: Galactosemia is a disorder that affects how the body processes a simple sugar called galactose. A small amount of galactose is present in many foods. It is primarily part of a larger sugar called lactose, which is found in all dairy products and many baby formulas. The signs and symptoms of galactosemia result from an inability to use galactose to produce energy.Classic galactosemia, also known as type I, is the most common and most severe form of the condition. If infants with classic galactosemia are not treated promptly with a low-galactose diet, life-threatening complications appear within a few days after birth. Affected infants typically develop feeding difficulties, a lack of energy (lethargy), a failure to gain weight and grow as expected (failure to thrive), yellowing of the skin and whites of the eyes (jaundice), liver damage, and abnormal bleeding. Other serious complications of this condition can include overwhelming bacterial infections (sepsis) and shock. Affected children are also at increased risk of delayed development, clouding of the lens of the eye (cataract), speech difficulties, and intellectual disability. Females with classic galactosemia may develop reproductive problems caused by an early loss of function of the ovaries (premature ovarian insufficiency). Galactosemia type II (also called galactokinase deficiency) and type III (also called galactose epimerase deficiency) cause different patterns of signs and symptoms. Galactosemia type II causes fewer medical problems than the classic type. Affected infants develop cataracts but otherwise experience few long-term complications. The signs and symptoms of galactosemia type III vary from mild to severe and can include cataracts, delayed growth and development, intellectual disability, liver disease, and kidney problems.
