Haem Flashcards

1
Q

Causes of increased red call degeneration

A
Hereditary spherocytosis
G6PD deficiency
Sickle cell disease
Thalassaemia
Haemolytic disease of the new-born
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2
Q

Causes of extensive blood loss in babies which leads to anaemia

A

von Willebrand

Merkel diverticulum

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3
Q

Causes of poor red cell production anaemia

A
Iron deficiency
Folic acid deficiency
Chronic renal failure
Diamond-Blackfan anaemia
Parvovirus B19 infection
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4
Q

Cause of anaemia if reticulocyte count is high or low?

A
High = increased destruction/haemolysis or blood loss.
Low = lack of production of RBC
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5
Q

Physiological anaemia of the new-born

A

Hb decreased from birth as RBC production is low, shorter RBC life span and switch from HbF to HbA

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6
Q

Most common cause of anaemia in children

A

Iron deficiency.

Present with palloe, irritability, anorexia, TC, cardiac murmur and cardiac dilation.

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7
Q

Microscopy of iron deficiency anaemia

A

Microcytic and Hypochromic

Low ferritin, low iron, increased TIBC

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8
Q

Other features of sickle cell disease apart from anaemia

A
Strokes
Infection/sepsis
Pain crisis
Acute chest syndrome
Dactylitis
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9
Q

Normal globin chain

A

alpha2 beta2

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10
Q

Asymptomatic thalassaemia

A

beta minor

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11
Q

Clinical features of hereditary spherocytosis

A
Autosomal dominant mostly
Jaundice
Anaemia
Splenomegaly
Gallstones
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12
Q

Congenital red cell aplasia

A

Diamond-Blackfan anaemia

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13
Q

Genetics of G6PD

A

X-linked

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14
Q

Acute bruising, purpura, petechiae
History of URTI
No organomegaly

A

Idiopathic thrombocytopenic purpura

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15
Q

Inheritance of haemophilia

A

X-linked

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16
Q

CFx of haemophilia

A

Recurrent bleeds into joints
Arthritis
High activated partial thromboplastin time

17
Q

Difference between haemophilia A and B

A
A = deficiency in factor 8
B = deficiency in factor 9
18
Q

Functions of von Willebrand factor

A

Helps platelet adhesion

Carrier protein for factor 8C

19
Q

Other Rx apart from recombinant factor8 for haemophilia A

A

Desmopressin

20
Q

Inheritance of von Willebrand disease

A

Autosomal dominant

21
Q

CFx of von Willebrand disease

A

Bruising, epistaxis, primary menorrhagia