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BIOCHEM
BIOCHEM
A sweat test measures the amount of chloride in sweat. Chloride is part of the salt that's
found in sweat. The test can diagnose cystic fibrosis (CF) because people with CF have
higher levels of chloride in their sweat. CF is an inherited disease that can affect people
of all ages. To have cystic fibrosis, you must inherit a changed CFTR gene from both
your parents. (Changes in genes are also called variants or mutations.) If you inherit
one changed gene, you won't have the disease, but you will be a carrier. Being a carrier
means that if you have children with someone who also has changes in one or both of
their CFTR genes, your children could inherit two changed genes and have CF.
PROCEDURE
1. Selectanarea
2. Apply iodine in designated area
3. Put a starch
4. Wait a atleast 20 mins for the result
PROCEDURE
1. Extract blood
2. Wait for the serum/plasma to settle
3. Transfer the serum to two tube
4. Tube A will be having the 0.5 ml starch solution 2-3 drops of iodine
5. Tube B will be having no starch solution 2-3 drops of iodine
Post question
1. What is the main purpose of the starch test in the sweat glands?
-In order to do a starch test, you must wet a portion of your body—usually your palm—
with iodine and then sprinkle starch powder over it. The primary goal of a starch test
performed on the sweat glands is to locate the area of the skin where persistently high
sweating occurs.
6. What are the diseases that can be detected by using a starch test?
-A starch test can be used to identify or diagnose certain diseases, such as Horner
syndrome. Clinical signs of the syndrome include ipsilateral drooping eyelids,
decreased sweating on the afflicted side of the body, and decreased pupil size, which is
worsened in scotopic conditions. In addition, the iodine-starch test is an excellent
diagnostic tool for Horner syndrome.