Biology, asked by sreeharims, 3 months ago

How do we detect a disease?​

Answers

Answered by aafiakhan07
1

Answer:

Blood tests. A technician obtains a sample of blood by inserting a needle into a vein, usually in the arm.

Urine tests. This painless test requires you to urinate into a container. To avoid potential contamination of the sample, you may be instructed to cleanse your genital area with an antiseptic pad and to collect the urine midstream.

Throat swabs. Samples from the throat, or other moist areas of the body, may be obtained with a sterile swab.

Stool sample. You may be instructed to collect a stool sample so a lab can check the sample for parasites and other organisms.

Spinal tap (lumbar puncture). This procedure obtains a sample of the cerebrospinal fluid through a needle carefully inserted between the bones of the lower spine. You'll usually be asked to lie on your side with your knees pulled up toward your chest.

Answered by jayasriskp
1

Answer:

We detect a disease almost by their symptoms. Some of them need tests to be confirmed, while some of them do not.

For Example: Let us take Covid-19. Even though we have symptoms, we may have same symptoms for other disease also. To get confirmed, we need to have a test.

Now let's take another example: common cold. It do not need any tests. The Symptoms confirm it is so.

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