Answer:
1. Integrity
2. Health Care
3. Code of Ethics
Explanation:
I calculated it logically
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.
<u>Dyslexia</u> is a developmental disorder with which reading achievement is substantially lower than predicted by IQ or age.
This condition varies from person to person as some have trouble reading swiftly and some reads without making mistakes. Dyslexia is a neurological disorder and it can run into families (hereditary).
It is so because it is an erudition/learning difficulty that diminishes a person’s potential to read and write. As in this disorder a person brain processing and efficiency gets weaken for written matters, making it more difficult to identify, spell, and decode the words. It is not something which can't be treated as there are several cases to be found in young ones and adults as well.
To learn more about Dyslexia here
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