Answer:
Elevate the arm, cover the wound with a dressing and apply pressure
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:
a pulmonary embolism.
Explanation:
A sudden onset of difficulty breathing, sharp chest pain and cyanosis that persists despite supplemental oxygen is most consistent with<u> a pulmonary embolism.</u>
Answer:
a. Monocytes
Explanation:
Monocytes
It is the agranulocytes and are capable of amoeboid movement and phagocytosis .
The main function of monocyte is as follows -
- The main function of monocyte is phagocytosis , antigen presentation and the production of cytokinin .
- These cells are known as amoeboids as they exhibit amoeboid movement .
Answer:
<h3>
the lacrimal gland</h3>
Explanation:
<em>It is secreted by the </em><em>lacrimal gland</em><em> on the underside of the upper eyelid. In addition, mucus mucin (secretory mucin), which is secreted by the goblet cells on the surface of the eye, helps distribute tears across the surface of the eye uniformly</em>
