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What is a heterozygous B-thalassemia? Question 10 (Mandatory) (1 point) A serum ferritin level on a patient...

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Question

Biology

What is a heterozygous B-thalassemia?

Question 10 (Mandatory) (1 point)

A serum ferritin level on a patient with a slight microcyticanemia due to a chronic disease will typically be___________________.

Question 10 options:

normal

decreased

increased

Question 11 (Mandatory) (1 point)

Another name for a siderotic, or iron, granule is a________________________.

Question 11 options:

Howell-Jolly Body

Heniz Body

Pappenheimer Body

Polychromasia

Question 12 (Mandatory) (1 point)

The test which evaluates the binding ability of transferrin isthe _____________________ test.

Question 12 options:

serum ferritin

serum iron level

TIBC

folate level

Question 13 (Mandatory) (1 point)

Most of the iron stored in the body is stored as__________________.

Question 13 options:

ferric iron

ferritin

hemosiderin

Howell-Jolly bodies

Question 14 (Mandatory) (1 point)

The ferritin level in Sideroblastic anemia would be__________________.

Question 14 options:

normal

decreased

increased

Question 15 (Mandatory) (1 point)

Which of the following would be seen in SideroblasticAnemia?

Question 15 options:

an M:E ratio of 6:1

a negative Prussian Blue

ringed sideroblasts in the bone marrow

an RDW of 16.0

Answer & Explanation Solved by verified expert
4.4 Ratings (671 Votes)
Ans heterozygous beta thalessemia is a congenital blood dyscrasia which occurs due to lack of beta globin chain in hemoglobin molecule causing microcytic hypochromic anemia This anemia is mild since the gene coding are hetrozygous Q10 decreased Microcytic anemia are generally seen in iron deficiency anemia sideroblastic anemia anemia of inflammation or chronic fisease amd    See Answer
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