Introduction to Hematology Flashcards

1
Q

The cellular component of blood makes up_____% of its volume.

A

40-45

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2
Q

when is anticoagulant added in a blood test and why?

A

when blood is drawn. It is added to the test tube or else the blood will clot in the tube.

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3
Q

To make Hemoglobin S what kind of mutation is needed?

A

Glu–>Val at the 6th position of the beta-globin chain. (it hurts when you get cold with sickle cell anemia so you have to put on your Glu-V).

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4
Q

Can RBCs make new RNA?

A

no they lack a nucleus. This means they have limited ability to respond to environmental changes or repair themselves.

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5
Q

If RBCs have no mitochondria how do they generate ATP energy?

A

anaerobic metabolism

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6
Q

what is porphyria?

A

mutation in the enzyme which forms the heme prosthetic group.

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7
Q

RBCs must have the ability to reduce reactive O2 that can accumulate in the cell. The most common disease which affects this enzyme is:

A

glucose 6 phosphate dehydrogenase (G6PD) deficiency. Like Sickle Cell it mostly affects Africans (males with this one though).

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8
Q

RBCs are shaped in a biconcave disk. What benefits does this afford the cell?

A

More surface area for gas exchange. Can manipulate shape easier to squeeze into tight areas.

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9
Q

Spherocytosis occurs when:

A

There is a mutation in the 2 dimensional elastic network of cytoskeletal proteins which tether sites on cytoplasmic domains of transmembrane proteins. This protein allows the cell to be elastic and reshape when squeezing through tight stuff.

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10
Q

Vitamin B12 and Folic Acid are necessary for a cell to ______.

A

undergo normal cell division.

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11
Q

Adaptive immune response is constituted mostly of ______.

A

lymphocytes.

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12
Q

Lymphocytes contribute to the development of immune memory. T or F?

A

T

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13
Q

Innate immunity is mostly done by what kind of cells?

A

myeloid.

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14
Q

CML is what chromosomes again?

A

9;22

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