Answer:
your answer would be sinus node (also called the sinoatrial node, or SA node).
Explanation:
The correct answer is letter B. The food molecules that cannot be digested need to be eliminated from the body. This can be done by taking in certain kinds of medicines that stimulate the digestive tract to pass out the food molecules that are indigestible.
Answer:
An 81-year-old male who has a productive cough, dyspnea and hypoxia
Explanation:
Chronic obstructive pulmonary disease (COPD) is the obstruction of airflow through the lungs usually caused by cigarette smoke or other harmful compounds. The disease appears after a persistent bronchitis or pulmonary emphysema. It causes a permanent state of inflammation in the lungs and it destroys the alveoli (structures that promote gas exchange in the organ).
The condition is dangerous because, in addition to the potential to stop breathing once and for all, it decreases the circulation of oxygen in the blood and triggers inflammatory substances throughout the body. The risk of heart attack and stroke get even higher. Patients may also suffer from muscle weakness, impaired thinking, and even more depression. Despite of being frequently associated with smoking, about one third of those with COPD never smoked.
The symptons usually are: productive cough
, throat clearing
, shortness of breath and fatigue and excessive phlegm. Dyspnea is progressive, persistent, stress-related or worsening in the presence of respiratory infection eventually arises at the time the patient.
ANSWER:
Phenylketonuria children are advised to avoid specific foods due to a dysfunction in the degradation of amino acids that contains phenylalanine.
Explanation:
Phenylalanine is one of the amino acids that can be found in specific foods like protein diet. Phenylalanine ought to be broken down in a form that the body can use for its normal activity. A dysfunction by the body to breakdown phenylalanine results in elevated levels which results in the condition known as phenylketonuria. Phenylketonuria is a genetic disorder that can be inherited, in which the body lacks an enzyme known as phenylalanine hydroxylase that is responsible for the break down of phenylalanine.
