anaemia Flashcards

1
Q

oxyhaemaglobin

A

oxygenated state of Hb

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2
Q

whats the functional form of Fe

A

Fe3+

fe atom remains in reduced form

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3
Q

how is Hb used as a buffer

A

H+ ions left over from dissociation of carbonic aci to bicarbonate bind to globin chains of Hb
Hv maintains the stable plasma pH of 7

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4
Q

role of band 3 protein

A

anion transport

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5
Q

role of glycophorin A

A

maintance of neg chaege

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6
Q

role of glycophorin C

A

regulates cell shape and membrane stability

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7
Q

role of ankyrin

A

links lipids to spectrin

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8
Q

spectrin role

A

maintence of biconcav disc

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9
Q

common symptoms of anaemia

A
short breath
weakness
pallor
llethargy
palpitations
headaches
confusion
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10
Q

clinical signs of anaemia

A
concave nails
jaundice
leg ulcers
bone defomaties
recurrent infections
bruising
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11
Q

normal value for mean cell volume

A

80-101

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12
Q

normal vlaue for mea cell Hb MCH

A

27-34

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13
Q

normal value for mean corpuscular Hb concentration MCHC

A

300-350

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14
Q

classifications of anaemia by cell size

A

microcytic
normoctyic
macrocytic

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15
Q

classification of anaemia by Hb

A

hypochromic
normochromic
hyperchromic

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16
Q

other extra classifications of anaemia

A

imparied production

loss of RBC or destruction

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17
Q

what is normocytic normochomic anaemia

A

RBC normal vol normal amount of Hb and normal concentration

BUT count is low

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18
Q

causes of normocytic and normochromic anaemia

A

acute bleed
marrow failure
haemolysis
renal failure, EPO deficiency

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19
Q

what is microcytic hypochromic anaemia

A

RBC low volum
low concentration Hb
less Hb too
low MCV MCH and MCHC

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20
Q

causes of microcytic hypochromic anaemia

A

Fe deficiency

thalassemia

21
Q

what is macrocytic normochrmic anaemia

A
RBC could low
RBC increased volume
Hb normal 
- MCV increased
-MCHC normal
- MCH increased
22
Q

causes of macrocytic normochromic anaemia

A

b12 or folate deficiency

23
Q

clinical causes of anaemia and red cell diseases

A
  • bleeding
  • b12/folate deficiency
  • RBC cytoskeletal disorders
  • impairment of erythropoiesis
  • acquired haemolyic anaemia
  • RBC enzympoathies
  • haemoaglobinophathy
24
Q

anaemis due toacute blood loss

A

normocytic normochonic anaemia

25
anamia due to iron deficiency
IDA microcytic hypochromic small, pale missshaped RBC
26
treatment of IDA
replenishment of iron, oral or injectios
27
anaemia caused by b12 or folate deficiency
macrocytic | normochromic
28
what are the types of cytoskeletal RBC disorders that can cause anaemia
1. hereditary elliocytosis | 2. heriditary spherocytosis
29
herditary ellipocytosis causing anaemia
cytoskeletal RBC disorder normocytic norochomic - spectrin, glycophorin C
30
hereditary spherocytosis causing anaemia
cytoskeletal RBC disroder normocytic, normochromic - spectrin, ankyrin, band 3
31
what are acquired impariments of erythropieisis
- bone marrow ilfiltration /cancers | - transient failure
32
what type of anaemia does impariment of erythrpoeisis cause
normocytic normochromic | tear-drop poililocytes
33
what are the two types of inherited erythropoiesis
- fanconi anaemia | - diamon blackfan anaemia
34
what is fanconi anaemia
inherited impairment of erythropoiesis | progresive bone marrow failure
35
what are the types of aquired haemolytic anaemia
- autoimmune | - microangiopathic mechanical fragmentation
36
what is autoimmune acquired haemolytic anaeia
normocytic normocromic anaemia | idiopathic but might be drug induced
37
what is microangiopathic anaemia
acquired haemolytic anaemia associiated with mechanican heart values - normocytic and normochromic
38
congenital haemolytic anaemia types
RBC enzympoathies normoc`qytic normchomic cellular dehydration haemolysis occurs
39
what is haemoglobinopathy?
2 categories - strucural - thalasaemia
40
what is structural haemaglobinopathy
amino acid subsututions leading to changes | eg sickle cell anaemia
41
what is sickle cell anaemia
``` strucutral haemaglobinopathy normochomic normocytic polymorphism distored shap RBC can be asympomatic of heterozygote ```
42
why is sickle cell anaemia called a balanced polymorphism
heterozygote with the disease will be more fit than a homzygote
43
thalasaemia haemoglobinopathy
group of inherited RBC disorders | characterised by reduced globin chain synthesis
44
what is alpha thalasaemia
inability to synthesise alpha globin chains | mild microcytic hypochromic anaemia
45
what is beta thalassamiia
impaired synthsis of beta globin chains | leads to ineffective erythropoiesis and reduced RBC survival, cleared by spleen
46
examples of normocytic normochomic anaemia
bleeding haemolysis drug induced anaemia strucutral variants of Hb
47
examples of microcytic hypochromic anaemia
fe deficiency thalassaemiae strucural variations
48
exaxples of macrocytic normochomic anaemia
B12/folate deficiency anaemia due to alcholism blackfan diamond