Chief of the hospital because they make or break the hospital they get all the orders and surgeons they make sure the hospital keeps running
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.
The period of gestation that is characterized by the largest fetal weight gain and fat deposition is the third trimester.
The third trimester is the last phase of gestation. It lasts for weeks 29 to 40, or months 7, 8, and 9.The baby grows, develop, and begins to change position in preparation for birth during this trimester. By the end, a full-term infant usually is between 19 and 21 inches long and between 6 and 9 pounds.
Pregnancy causes major physical and psychological changes in women. Weight gain during the third trimester is a normal part of pregnancy and typically not a reason for concern.
During the third trimester, many women will gain weight quickly. This is because, according to the Office on Women's Health (OWH)Trusted Source, the fetus normally accumulates the most weight during this time.
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When preparing a multigravid client who has undergone evacuation of a hydatidiform mole for discharge, the nurse explains the need for follow-up care and the client is said to understand it when she says that she is at risk for developing choriocarcinoma.
<h3>What is Choriocarcinoma?</h3>
This is defined as a medical condition which is characterized by a fast-growing cancer that occurs in a woman's uterus. This type of cancer affects the placenta in most situations and it is the organ which supplies food and other nutrients from the woman to the fetus.
In a situation where the individual had hydatidiform mole which is the abnormal growth of trophoblasts which are tissues which form the placenta then there is a likelihood of her having choriocarcinoma in this scenario.
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