Answer:
The part of the environment that is most crucial to the development of skin pigmentation overhuman development and across geographic locations is the intensity
Explanation:
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.
Answer:
Histamine, is the chemical mediator initiates an inflammatory reaction. An inflammatory mediator is basically defined as that act in blood vessels and cells for promote response of inflammatory mediator. Histamine is the main chemical mediator which are released from the cells during inflammation, which increases vascular permeability. It is stored in granules and mast cells and get released immediately when the cells get injured.
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His symptoms severely limited his ability to function and caused him to avoid leaving the house, so the nurses recognized that this client had symptoms of 4. agoraphobia.
<h3>What is agoraphobia?</h3>
Agoraphobia is a type of anxiety disorder. This disorder causes excessive feelings of fear and worry when in a place that makes it difficult for the sufferer to leave or feels unable to ask for help from anyone.
The causes of agoraphobia are still not known with certainty. However, this phobia is more prone to occur in people with a history of recurrent panic attacks. Although rare, agoraphobia can also occur in people who don't have a history of panic attacks.
Learn more about the type of panic disorder here :
brainly.com/question/15089104
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