Answer:
Let the patient speak. ... ...
Involve the family always. ...
Always ask open-ended questions
Answer:
illusions sorry for the late answer
Answer:
The arguments for the Compassionate Use Act include the following:
1. The patient has an acute disease or health condition. Also, whose life is being threaten.
2. The patient is not allowed to enter a clinical trial.
3. The patient benefit supports the potential risks of treatment.
4. The patient has no other treatment therapy for the disease or health condition
5. The investigative outcome of the treatment should not interfere with any trials that could support a medical's product development or marketing approval for the treatment indicated.
Explanation:
Answer:
I had a migraine just trying to read this.
Explanation:
Answer: The brain i was born with is a fully sized brain
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.