Gastro Flashcards

(34 cards)

1
Q

Wilsons disaese

A

excessive deposition of copper in liver, brain, cornea and kidneys

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2
Q

inheritance of wilsons disease

A

autosomal recessive

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3
Q

blood test reults in wilson disease

A

low ceruloplasmin and total serum copper

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4
Q

mutation in wilson disease

A

ATP7B gene

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5
Q

symptoms of wilsons

A

dystonia, Parkinsonian tremor, rigidity with behavioural problems and dementia
Kayser Fleisher ring

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6
Q

physiological jaundice causes which type of hyperbilirulaemia

A

unconjugated

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7
Q

What is kernicterus

A

bilirubin encephalopathy

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8
Q

causes of kernicterus

A

acidosis, asphyxia, sepsis, prematurity

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9
Q

most common cause of diarrhoea

A

rotavitus (A in 90%)

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10
Q

common cause of food related gastroenteritis

A

campylobacter

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11
Q

GI infection that mimics appendicitis

A

Yersinia

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12
Q

when is rotavirus vaccine given

A

8-12 wks

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13
Q

when do rotavirus infections most commonly occur

A

november to april

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14
Q

treatment for mild, uncomplicated chron flareup

A

elemental diet
corticosteroids 1-2mg/kg/day
abx for perianal disease (metro and xipro)
aminosalicylates

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15
Q

when does pyloric stenosis present

A

2-4 wks of life with projectile vomiting

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16
Q

cause of pyloric stenosis

A

hypertrophy of muscles of pyloric sphincter leading to functional gastric outlet obstruction

16
Q

type of vomiting in pyloric stenosis

17
Q

risk factors for pyloric stenosis

A

FH (87% heritability)
male baby
first born
caucasia

18
Q

blood findings in pyloric stenosis

A

hypokalaemic metabolic alkalosis

19
Q

diagnosis of pyloric stenosis

20
Q

management of pyloric stenosis

A

ramstedt procedure

21
Q

what is the procedure indicated in biliary atresia

22
Q

what is biliary atresia

A

progressive fibrosing obstructive cholangiopathy involving both extrahepatic and intrahepatic biliary system

23
Q

diagnostic procedure for biliary atresia

24
management of biliary atresia
fat soluble vitamins ursodeoxycholic acid nutritional support surgery
25
type of hyperbilirubinaemia in biliary atresia
conjugated
26
what is gilberts syndrome
benign, inherited liver disorder leading to intermittent episodes of mild jaundice due to high unconjugated bilitubin levels
27
what enzyme causes gilberts syndrome
glucuronyltransferase
28
what is hirshsprungs disaese
missing parasympathetic gangòlion cells in the muscles of part or all of the rectum - cannot relax and lead to obstruction
29
symptoms of Hirschsprungs
delayed passage of meconium (typically passed within 48hrs)
30
gender incidence of hirschsprungs
2-4 more common in males
31
what types of hernia are common in boys
indirect inguinal hernias
32
when should surgery take place for hernia
as soon as possible
33
whats the most common type of hernia
indirect inguinal