4th
i took quiz you are welcome
A psychosomatic disease is best defined as a disease in which
there are no observable symptoms.
mental factors do not affect overall health.
the body and mind contribute to an illness.
stress is unrelated to physical conditions.
Answer:
Body and mind contribute to the illness
Explanation:
On what does the World Health Organization base its standards?
research
first–hand observations
what other organizations are doing
solutions that make the most money
Answer:
Its research
Explanation:
I got it right in edge
true or false
gestational diabetes is indicated by a decrease in blood or urine glucose levels
Answer:
That is false
Because pregnancy causes the body’s need for energy to change, blood sugar levels can change very quickly
50 points brainliest I'm watching to wait explain the difference between essential body fat and storage body fat
What is the purpose of medical ethics?
Aaron, a healthcare worker, washed his hands, gave a patient a needle injection, and then disposed of the needle in a sharps container. Which best describes the error Aaron made in following standard precautions?
A. He should have placed the needle in the biohazards bin.
B. He should have put gloves on before working with the needle.
C. He should have contacted the CDC to report the use of a needle.
D. He should have checked the MSDS before disposing of the needle.
Answer: the answer is B
5. LSD is produced from ergot, a fungus that is found on some plants and grasses.
True
False
Answer:
That would be true.
Explanation:
Choose the correct location and hand placement to perform abdominal thrusts on a choking child
Answer:Stand or kneel behind the child and wrap your arms around his or her waist.
Explanation:
7. Hip dysplasia is an abnormal growth of the bones of the hip joint.
O
True
O
False
Answer:
brainliest plsssss
Explanation:
Hip dysplasia is an abnormality of the hip joint where the socket portion does not fully cover the ball portion, resulting in an increased risk for joint dislocation. Hip dysplasia may occur at birth or develop in early life. Regardless, it does not typically produce symptoms in babies less than a year old.
Other names: Developmental dysplasia of the ...
Risk factors: Family history, swaddling, breech ...
It is recommended that women of childbearing age take folic acid daily for prevention of a. neural tube defects. b. hydrocephalus. c. cerebral palsy. d. seizure disorders.
Answer:
A
Explanation:
to help prevent neural tube defects (NTDs). NTDs are major birth defects of the baby's brain (anencephaly) and spine (spina bifida).
Many people who are in favor of alternative medicine claim that large doses of vitamin C introduced into a vein speed up the healing of surgical wounds. Describe an experiment to test this hypothesis by answering questions 1-4
The game starts when one person serves from anywhere behind the __________.
Group of answer choices
back row
sideline
baseline
anywhere
Answer:
baseline
Explanation:
l think hope that helps
Select all that apply.
Which of the following statements are true about the genetic disease phenylketonuria?
It is not tested for until a person has symptoms later in life.
Untreated phenylketonuria can lead to brain damage.
Phenylketonuria is effectively treated with gene therapy.
It requires lifelong treatment.
Prenatal surgery is used to treat it.
Answer:
Untreated phenylketonuria can lead to brain damage.
It requires lifelong treatment.
Explanation:
The statements that are true about the genetic disease phenylketonuria are:
-Untreated phenylketonuria can lead to brain damage.
-It requires lifelong treatment.
What is Phenylketonuria?
Phenylketonuria (PKU) is a rare genetic disorder that affects the metabolism of the amino acid phenylalanine. People with PKU are unable to properly break down phenylalanine, an amino acid found in many protein-rich foods, as a result, the amino acid and its by-product, phenylpyruvic acid (PPA) builds up to harmful levels in the body, leading to intellectual disability, behavioral problems, and other serious health problems. PKU is caused by a mutation in the gene that codes for the enzyme phenylalanine hydroxylase (PAH), which normally converts phenylalanine to tyrosine.
The disorder is inherited in an autosomal recessive pattern, which means that a person must inherit two copies of the mutated gene, one from each parent, to develop the condition. PKU is usually diagnosed soon after birth by newborn screening, it is not typically tested for until a person has symptoms later in life. The treatment for PKU is a low phenylalanine diet, it requires lifelong treatment.
Learn more about Phenylketonuria, here:
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