Pediatric Pathology 3 Flashcards

1
Q

What’s the types of hyperbilirubinemia?

A
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2
Q

Discuss predominantly unconjugated hyoerbilirubinemia

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3
Q

Discuss predominantly conjugated hyperbilirubinemia

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4
Q

Discuss the physiological neonatal jaundice

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5
Q

Discuss pathological neonatal jaundice

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6
Q

Discuss the hemolytic disease of newborn

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7
Q

Describe the pathological features of hemolytic disease in a newborn

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8
Q

Discuss the diagnosis of hemolytic disease of newborn

A
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9
Q

Discuss treatment & prevention of hemolytic disease of a newborn

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10
Q

Discuss type 1 Crigler Najjar Syndrome

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11
Q

Discuss type 2 Crigler Najjar Syndrome

A
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12
Q

Describe biliary atresia

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13
Q

Discuss embryonal/fetal type biliary atresia

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14
Q

Discuss perinatal type biliary atresia

A

Etiology: Nornally developed biliary tree is destroyed following birth by a virus induced injury to biliary epithelium

Onset of cholestasis: late (4-8 weeks)

Jaundice free period after physiological jaundice: present

Associated congenital anomalies: absent

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15
Q

Discuss the morphology of biliary atresia

A
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16
Q

Discuss the prognosis of biliary atresia

17
Q

Discuss idiopathic neonatal hepatitis

18
Q

Discuss the epidemiology, clinical features and prognosis of idiopathic neonatal hepatitis

19
Q

Discuss the morphology of idiopathic neonatal hepatitis

20
Q

What is Dubin-Johnson Syndrome?

21
Q

Describe the etiopathogenesis of Dublin-Johnson syndrome

22
Q

Discuss the clinical features Dubin-Johnson syndrome

23
Q

Discuss the morphology of Dublin Johnson syndrome

24
Q

What is rotor syndrome?

25
What are the clinical features & pathological findings of rotor syndrome?
26
What is Cystic fibrosis?
27
Discuss etiopathogenesis of Cystic fibrosis
28
What happens in the absence of CFTR?
29
What happens to the lungs in cystic fibrosis?
30
What does cystic fibrosis do to the pancreas?
31
How does cystic fibrosis affect the liver?
32
How does cystic fibrosis affected the reproductive tract?
33
How does cystic fibrosis affect the meconium ileus ?
34
Discuss the clinical features of cystic fibrosi
35
How do we diagnose cystic fibrosis?
36
What are the inborn errors of metabolism?