Answer:
ions, glucose and amino acids i think
don't get mad
Explanation:
Answer:
Make an observation.
Ask a question.
Form a hypothesis, or testable explanation.
Make a prediction based on the hypothesis.
Test the prediction.
Iterate: use the results to make new hypotheses or predictions.
Answer:
Explanation:
Galactosemia is an inherited metabolic disorder caused by changes, or mutations, in both copies of an individual’s GALT gene. In the majority of cases, children with galactosemia do not have parents with galactosemia. Mother and father separately are a silent carrier of the condition, which is expressed in the child (autosomal recessive inheritance).
Each individual has two copies of the GALT gene – one from father and one from mother. In case of any changes of these genes (mutations) that prevents the gene from working correctly. In order to inherit galactosemia, it is necessary for a child to have two GALT gene changes. In case of one GALT gene change there is no galactosemia.
Infants with galactosemia may be identified through newborn screening programs or by symptoms that present during the first few weeks of life. Untreated infants develop liver and kidney disease, cataracts in their eyes, and serious infections.
The answer to this question is the Snellen chart that will be used by the nurse to test the vision of the low income women. A Snellen chart is an eye chart used to measure the vision of the patients. Snellen charts should be placed at least 2.8 meters from the patient to test its visual acuity. This chart was developed by Herman Snellen.
<span>I would see x-rays, ultraviolet rays, and radio waves if my vision were “better.”</span>
