Answer:
1. Interpersonal
2. Punctuality
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.
Answer:
The correct answer is option C
FLANK PAIN AND HEMATURIA
A client has been diagnosed with polycystic kidney disease. On assessment of the client, the nurse will observe for FLANK PAIN AND HEMATURIA as the most common manifestation of this disorder
Explanation: Polycystic kidney disease is an inherited disease of the kidney caused by abnormal gene mutation, it is characterised by clusters of non cancerous sacs containing water-like fluids (cysts) in the kidney.
Symptoms of polycystic kidney disease includes back or side pain,swollen abdomen,excessive tiredness (fatigue), blood in the urine and high blood pressure.
Treatment of polycystic kidney disease is with administration of pain relievers, anti-hypertensive like angiotensin converting enzyme inhibitor(example;Captopril) to control blood pressure, avoidance of high sodium diet, surgical removal of cyst, haemodialysis and kidney transplantation.
The answer should be B) Stroke
True
Explanation:Whenever an acid donates a proton, the acid changes into a base, and whenever a base accepts a proton, an acid is formed. An acid and a base which differ only by the presence or absence of a proton are called a conjugate acid-base pair. ... Similarly, HF is the conjugate acid of F–, and F– the conjugate base of HF
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