Part 5- CHELATOR & HEAVY METALS

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Last updated 10:23 AM on 6/3/26
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111 Terms

1
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[CHELATOR]

DEFEROXAMINE

a. Cuprimine®

b. BAL

c. Desferal®

d. DMSA

c. Desferal®

2
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[CHELATOR]

Chelators are substances that contain:
a. a lone pair of electrons
b. free radicals only
c. positively charged metals
d. carbohydrates

a. a lone pair of electrons

3
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[CHELATOR]

Which functional groups commonly acts as a metal-binding site in chelators?


a. -NH
b. -CH₃
c. -SH
d. -OH

a. -NH
c. -SH
d. -OH

4
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[CHELATOR]

Deferoxamine is the drug of choice (DOC) for poisoning with:
a. lead
b. mercury
c. iron (Fe)
d. arsenic

c. iron (Fe)

5
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[CHELATOR]

Which route of administration can be used for deferoxamine?
a. IV
b. IM
c. SC
d. PO

a. IV
b. IM
c. SC

6
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[CHELATOR]

Deferoxamine binds primarily to:
a. ferrous iron (Fe²⁺)
b. ferric iron (Fe³⁺)

b. ferric iron (Fe³⁺)

7
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[CHELATOR]

The complex formed between deferoxamine and ferric iron is called:
a. cyanomethemoglobin
b. sulfmethemoglobin
c. carboxyhemoglobin
d. ferrioxamine

d. ferrioxamine

8
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[CHELATOR]

Ferrioxamine is primarily eliminated through:
a. feces
b. sweat
c. urine
d. bile

c. urine

9
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[CHELATOR]

Which iron-containing structure is NOT significantly bound by deferoxamine?
a. ferric iron stores
b. hemoglobin
c. free ferric iron
d. ferric iron complexes

b. hemoglobin

10
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[CHELATOR]

Deferoxamine does not significantly bind:
a. ferric iron
b. cytochromes
c. urinary iron
d. transferrin-bound iron

b. cytochromes

11
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[CHELATOR]

Dimercaprol (BAL) was originally developed for poisoning with:
a. arsenic gas
b. cyanide
c. iron
d. methanol

a. arsenic gas

12
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[CHELATOR]

Dimercaprol is effective in poisoning with:
a. arsenic, gold, and mercury
b. iron, calcium, and magnesium
c. sodium, potassium, and chloride
d. cyanide, carbon monoxide, and methanol

a. arsenic, gold, and mercury

13
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[CHELATOR]

Dimercaprol is administered via:
a. oral route
b. intravenous route
c. intramuscular route
d. subcutaneous route

c. intramuscular route

14
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[CHELATOR]

The vehicle used in dimercaprol injections is:
a. mineral oil
b. olive oil
c. peanut oil
d. castor oil

c. peanut oil

15
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[CHELATOR]

In severe lead poisoning, dimercaprol is commonly used with:
a. deferoxamine
b. calcium EDTA
c. penicillamine
d. methylene blue

b. calcium EDTA

16
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[CHELATOR]

Dimercaprol forms a stable complex known as:
a. ferrioxamine
b. dimercaptide
c. cyanomethemoglobin
d. carboxyhemoglobin

b. dimercaptide

= dimercaprol:metal

=2:1

17
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[CHELATOR]

What is the chelator-to-metal ratio in the dimercaptide complex?
a. 1:1
b. 1:2
c. 2:1
d. 3:1

c. 2:1

18
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[CHELATOR]

Which statement about dimercaprol toxicity is correct?
a. least toxic chelator
b. most toxic among chelators
c. no significant toxicity
d. safer than all other chelators

b. most toxic among chelators

19
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[CHELATOR]

Dimercaprol is indicated primarily for:
a. chronic poisoning only
b. acute poisoning only
c. prophylaxis only
d. food poisoning only

b. acute poisoning only

20
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[CHELATOR]

Median lethal dose of dimercsprol

a. 10 mmcl/kg
b. 0.1 mmcl/kg
c. 100 mmcl/kg
d. 1 mmcl/kg

d. 1 mmcl/kg

21
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[CHELATOR]

A common adverse effect of dimercaprol is:
a. decreased systolic and diastolic blood pressure by 50 mmHg
b. increased systolic and diastolic blood pressure by 10 mmHg
c. increased systolic and diastolic blood pressure by 50 mmHg
d. decreased systolic and diastolic blood pressure by 10 mmHg

c. increased systolic and diastolic blood pressure by 50 mmHg

22
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[CHELATOR]

Another common adverse effect of dimercaprol is:
a. pain at the injection site
b. blindness
c. renal stones
d. pulmonary fibrosis

a. pain at the injection site

23
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[CHELATOR]

Why is dimercaprol contraindicated in chronic arsenic poisoning?
a. causes iron deficiency
b. may redistribute arsenic from tissues to the brain
c. blocks renal excretion and severe hypotension
d. causes severe hypocalcemia

b. may redistribute arsenic from tissues to the brain

24
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[CHELATOR]

Dimercaprol (BAL) is contraindicated in poisoning with Cd, Se, Tc, Fe, and organomercurials because it:
a. decreases metal absorption
b. increases tissue uptake of these substances
c. blocks renal excretion completely
d. forms inactive complexes excreted in urine

b. increases tissue uptake of these substances

25
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[CHELATOR]

Which of the followings are contraindication to dimercaprol therapy?
a. arsenic poisoning
b. organomercurials
c. iron poisoning
d. fluorine poisoning

b. organomercurials &
c. iron poisoning

26
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[CHELATOR]

Dimercaprol should be avoided in poisoning with all EXCEPT:
a. cadmium
b. selenium
c. technetium
d. arsenic

d. arsenic

27
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[CHELATOR]

DIMERCAPTOSUCCINIC ACID aka
a. dimercaprol
b. BAL
c. succimer
d. DMSA

c. succimer &
d. DMSA

28
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[CHELATOR]

DIMERCAPTOSUCCINIC ACID / Succimer (DMSA) is best described as:
a. a water-soluble form of dimercaprol (BAL)
b. an iron chelator
c. a cyanide antidote
d. a nitrate antidote

a. a water-soluble form of dimercaprol (BAL)

29
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[CHELATOR]

The usual route of administration for succimer is:
a. IV
b. IM
c. SC
d. oral

d. oral

30
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[CHELATOR]

Succimer (DMSA) is particularly useful in:
a. acute poisoning
b. chronic poisoning
c. cyanide poisoning
d. carbon monoxide poisoning

b. chronic poisoning

  • DMSA- chronic poisoning

  • BAL- acute poisoning

31
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[CHELATOR]

D-Penicillamine is classified as a:
a. dithiol chelator
b. monothiol chelator

b. monothiol chelator

32
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[CHELATOR]

The usual route of administration for D-Penicillamine is:
a. IV
b. IM
c. SC
d. oral

d. oral

33
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[CHELATOR]

D-Penicillamine

a. Cuprimine®

b. BAL

c. Desferal®

d. DMSA

a. Cuprimine®

34
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[CHELATOR]

D-Penicillamine is the drug of choice (DOC) for:
a. iron toxicity
b. copper toxicity
c. lead toxicity
d. mercury toxicity

b. copper toxicity

35
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[CHELATOR]

D-Penicillamine is commonly used in the treatment of:
a. cyanide poisoning
b. methanol poisoning
c. methemoglobinemia
d. Wilson's disease

d. Wilson's disease

36
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[CHELATOR]

Besides copper, D-Penicillamine can also bind:
a. iron, mercury, lead, zinc, and arsenic
b. sodium, potassium, chloride, and arsenic
c. calcium, potassium, chloride and magnesium
d. carbon monoxide only

a. iron, mercury, lead, zinc, and arsenic

37
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[CHELATOR]

D-Penicillamine is contraindicated in patients with:
a. sulfa allergy
b. aspirin allergy
c. penicillin allergy
d. iodine allergy

c. penicillin allergy

38
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[CHELATOR]

Calcium EDTA binds:
a. monovalent metals
b. divalent and trivalent metals
c. tetravalent metals
d. nonmetal toxins

b. divalent and trivalent metals

39
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[CHELATOR]

Which route of administration is used for Calcium EDTA?
a. PO and IM
b. SC and PO
c. SC only
d. IV and IM

d. IV and IM

40
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[CHELATOR]

Calcium EDTA forms a complex that is:
a. water-soluble
b. lipid-soluble

a. water-soluble

41
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[CHELATOR]

The metal-Calcium EDTA complex is primarily eliminated through the:
a. lungs
b. liver
c. kidneys
d. skin

c. kidneys

42
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[CHELATOR]

Which heavy metal poisoning can be treated with Calcium EDTA?
a. lead (Pb)
b. carbon monoxide
c. cyanide
d. methanol

a. lead (Pb)

43
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[CHELATOR]

Calcium EDTA is also used in poisoning with:
a. cadmium, cobalt, copper, and zinc
b. sodium and potassium
c. fluoride and chloride
d. carbon dioxide and oxygen

a. cadmium, cobalt, copper, and zinc

44
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[CHELATOR]

The initial antidote of choice for severe lead poisoning is:
a. succimer with d-penicillamine
b. deferoxamine alone
c. calcium EDTA with BAL
d. penicillamine alone

c. calcium EDTA with dimercaprol (BAL)

45
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[HEAVY METALS]

The common mechanism of toxicity of heavy metals is:
a. stimulation of sulfhydryl (-SH) groups of enzymes, causing activation
b. stimulation to (-NH) groups of enzymes, causing activation
c. binding to (-NH) groups of enzymes, causing inactivation
d. binding to sulfhydryl (-SH) groups of enzymes, causing inactivation

d. binding to sulfhydryl (-SH) groups of enzymes, causing inactivation

46
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[HEAVY METALS]

The main treatment for heavy metal poisoning involves:
a. anticholinergics
b. chelators (chelating agents)
c. anticonvulsants
d. antihistamines

b. chelators (chelating agents)

47
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[HEAVY METALS]

Chelator-heavy metal complexes are generally:
a. lipid-soluble
b. protein-bound
c. water-soluble
d. insoluble

c. water-soluble

48
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[HEAVY METALS]

Lewisite metal

a. LEAD
b. COPPER
c. ZINC
d. ARSENIC

d. ARSENIC

49
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[HEAVY METALS]

Salvarsan

a. LEAD
b. COPPER
c. ZINC
d. ARSENIC

d. ARSENIC

50
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[HEAVY METALS]

Arsphenamine

a. LEAD
b. COPPER
c. ZINC
d. ARSENIC

d. ARSENIC

51
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[HEAVY METALS]

Compound 606

a. LEAD
b. COPPER
c. ZINC
d. ARSENIC

d. ARSENIC

52
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[HEAVY METALS]

Magic Bullet

a. LEAD
b. COPPER
c. ZINC
d. ARSENIC

d. ARSENIC

53
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[HEAVY METALS]

A characteristic finding in acute arsenic poisoning is:
a. garlic odor on the breath
b. cherry-red skin
c. jaundice
d. hematuria

a. garlic odor on the breath

54
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[HEAVY METALS]

Which gastrointestinal manifestation is common in acute arsenic poisoning?
a. constipation
b. diarrhea

b. diarrhea = dehydration

55
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[HEAVY METALS]

Which CNS manifestation may occur in acute arsenic poisoning?
a. delirium
b. myopia
c. tinnitus
d. aphasia

a. delirium

56
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[HEAVY METALS]

Severe acute arsenic poisoning may progress to:
a. seizure and coma
b. cirrhosis only
c. nephrolithiasis only
d. bronchospasm

a. seizure and coma

57
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[HEAVY METALS]

A classic sign of chronic arsenic poisoning is:
a. Aldrich-Mee's lines
b. Koplik spots
c. Roth spots
d. Janeway lesions

a. Aldrich-Mee's lines

58
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[HEAVY METALS]

Aldrich-Mee's lines, from chronic arsenic poisoning, are described as:
a. white lines on the nails
b. blue lines on the gums
c. red lines on the skin
d. black streaks on the hair

a. white lines on the nails

59
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[HEAVY METALS]

Which skin finding may occur in chronic arsenic poisoning?
a. keratosis
b. urticaria
c. cyanosis
d. petechiae

a. keratosis

60
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[HEAVY METALS]

Which hair-related manifestation is associated with chronic arsenic poisoning?
a. excessive hair growth
b. hair loss
c. hair pigmentation
d. brittle nails

b. hair loss

61
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[HEAVY METALS]

Chronic arsenic poisoning may produce a:
a. milky and rosy complexion
b. jaundiced complexion
c. cyanotic complexion
d. bronze complexion

a. milky and rosy complexion

62
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[HEAVY METALS]

Chronic arsenic poisoning may lead to:
a. Abnormal weigh gain
b. Abnormal weight loss

a. Abnormal weigh gain

63
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[HEAVY METALS]

The chelator of choice for arsenic poisoning is:
a. deferoxamine
b. dimercaprol (BAL)
c. calcium EDTA
d. methylene blue

b. dimercaprol (BAL)

64
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[HEAVY METALS]

In severe arsenic poisoning, treatment may include:
a. BAL + penicillamine
b. deferoxamine + leucovorin
c. methylene blue + atropine
d. naloxone + flumazenil

a. BAL + penicillamine

65
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[HEAVY METALS]

Which of the following is a common source of lead exposure?
a. leaded gasoline
b. distilled water
c. table sugar
d. oxygen tanks

a. leaded gasoline

66
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[HEAVY METALS]

Lead may also be found in:
a. paint
b. antihistamines
c. vaccines
d. newspapers

a. paint &

d. newspapers

67
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[HEAVY METALS]

Lead may also be found in:
a. silver utensils
b. wire conductors
c. earthenware
d. automobile exhaust

c. earthenware &
d. automobile exhaust

68
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[HEAVY METALS]

The approximate half-life of lead in bone is:
a. 32 days
b. 32 months
c. 32 years
d. 3.2 years

c. 32 years

  • T1/2 (Bones) - 32 years

  • T1/2 (Kidneys) - 7 years

69
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[HEAVY METALS]

The approximate half-life of lead in the kidneys is:
a. 7 days
b. 7 months
c. 7 years
d. 70 years

c. 7 years

  • T1/2 (Bones) - 32 years

  • T1/2 (Kidneys) - 7 years

70
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[HEAVY METALS]

Lead toxicity causes anemia primarily by:
a. increasing erythropoietin production
b. interfering with heme synthesis
c. stimulating hemoglobin synthesis
d. increasing iron absorption

b. interfering with heme synthesis

71
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[HEAVY METALS]

Lead poisoning can result in anemia because it:

a. Increases RBC destruction and cytochrome production
b. Decreases platelet production
c. Interferes with heme synthesis and cytochrome production
d. Causes vitamin B12 deficiency

c. Interferes with heme synthesis and cytochrome production

72
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[HEAVY METALS]

A classic peripheral blood smear finding in lead poisoning is:

a. Heinz bodies
b. Spherocytes
c. Basophilic stippling
d. Schistocytes

c. Basophilic stippling

73
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[HEAVY METALS]

The gingival discoloration seen in chronic lead poisoning is called:

a. Koplik spots
b. Burton's line
c. Bitot spots
d. Roth spots

b. Burton's line

74
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[HEAVY METALS]

Which combination is most characteristic of lead poisoning?

a. Hemolytic anemia + Heinz bodies
b. Megaloblastic anemia + hypersegmented neutrophils
c. Anemia + basophilic stippling + Burton's line
d. Polycythemia + thrombocytosis

c. Anemia + basophilic stippling + Burton's line

75
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[HEAVY METALS]

Lead inhibits which two key enzymes in heme synthesis?

a. Ferrochelatase and ALA dehydratase
b. Cyclooxygenase and lipoxygenase
c. Glucokinase and hexokinase
d. MAO and COMT

a. Ferrochelatase and ALA dehydratase

76
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[HEAVY METALS]

Lead poisoning prevents:

a. Formation of bilirubin
b. Incorporation of iron (Fe) into protoporphyrin IX
c. Absorption of vitamin B12
d. Production of erythropoietin

b. Incorporation of iron (Fe) into protoporphyrin IX

77
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[HEAVY METALS]

Basophilic stippling in lead poisoning results from inhibition of:

a. Ferrochelatase
b. ALA synthase
c. 3',5'-Pyrimidine nucleotidase
d. Carbonic anhydrase

c. 3',5'-Pyrimidine nucleotidase

78
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[HEAVY METALS]

A child with lead poisoning is most likely to present with:

a. Hyperactivity and improved IQ
b. Encephalopathy with decreased IQ
c. Hyperthyroidism
d. Polycythemia

b. Encephalopathy with decreased IQ

79
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[HEAVY METALS]

Which neurologic finding is classically associated with lead toxicity?

a. Bell's palsy
b. Wrist drop
c. Hemiballismus
d. Nystagmus

b. Wrist drop

  • Peripheral neuropathy – wrist / foot drop

80
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[HEAVY METALS]

Which of the following may occur in severe lead encephalopathy?

a. Ataxia
b. Delirium
c. Coma
d. Seizure

a. Ataxia
b. Delirium
c. Coma

81
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[HEAVY METALS]

Chronic lead nephropathy may lead to:

a. Diabetes insipidus
b. Saturnine gout
c. Nephrotic syndrome
d. Renal stones

b. Saturnine gout

82
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[HEAVY METALS]

The classic gingival finding in lead poisoning is:

a. Koplik spots
b. Burton's line
c. Bitot spots
d. Roth spots

b. Burton's line

83
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[HEAVY METALS]

Initial treatment of severe lead poisoning commonly includes:

a. Naloxone + atropine
b. Pralidoxime + atropine
c. Flumazenil + N-acetylcysteine
d. CaNa₂EDTA + BAL

d. CaNa₂EDTA + BAL

84
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[HEAVY METALS]

The duration of initial treatment with CaNa₂EDTA + BAL should not exceed:

a. 24 hours
b. 3 days
c. 5 days
d. 14 days

c. 5 days

85
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[HEAVY METALS]

Which oral chelating agent is used for lead poisoning?

a. Succimer (DMSA)
b. Methimazole
c. Deferoxamine
d. Acetazolamide

a. Succimer (DMSA)

86
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[HEAVY METALS]

Which oral chelating agent is used for lead poisoning?

a. Deferoxamine
b. Methimazole
c. DMPs
d. Acetazolamide

c. DMPs

87
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[HEAVY METALS]

Cadmium poisoning is classically associated with:

a. Minamata disease
b. Wilson's disease
c. Itai-itai disease
d. Mad Hatter's disease

c. Itai-itai disease

88
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[HEAVY METALS]

The mechanism of toxicity of cadmium is:

a. Inhibition of MAO
b. Displacement of Ca²⁺ in bones
c. Inhibition of heme synthesis
d. Free radical scavenging

b. Displacement of Ca²⁺ in bones

89
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[HEAVY METALS]

Which bone disorder is commonly seen in cadmium poisoning?

a. Osteopetrosis
b. Osteomalacia
c. Osteoarthritis
d. Osteomyelitis

b. Osteomalacia

90
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[HEAVY METALS]

Cadmium toxicity may cause a Fanconi-like syndrome characterized by:

a. Proteinuria, aminoaciduria, glucosuria
b. Hematuria, pyuria, ketonuria
c. Polycythemia, thrombocytosis
d. Hypernatremia, hypokalemia

a. Proteinuria, aminoaciduria, glucosuria

91
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[HEAVY METALS]

A patient with cadmium poisoning is most likely to have:

a. Increased phosphate reabsorption
b. Decreased phosphate reabsorption
c. Hypercalcemia
d. Hyperuricemia

b. Decreased phosphate reabsorption

92
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[HEAVY METALS]

Which treatment is used for cadmium poisoning?

a. BAL
b. Deferoxamine
c. EDTA
d. Atropine

c. EDTA

93
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[HEAVY METALS]

Gait disturbances (abnormalities in walking patterns) is associated with this toxicity

a. CADMIUM
b. IRON
c. Cu
d. Hg

a. CADMIUM

94
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[HEAVY METALS]

Mercury is also known as:

a. Quicksilver
b. White lead
c. Calomel blue
d. Cinnabar

a. Quicksilver

95
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[HEAVY METALS]

Mercury poisoning is associated with:

a. Itai-itai disease
b. Wilson's disease
c. Minamata disease
d. Saturnism

c. Minamata disease

96
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[HEAVY METALS]

The mechanism of toxicity of mercury is:

a. Inhibition of ferrochelatase
b. Inhibition of MAO
c. Displacement of calcium
d. Inhibition of acetylcholinesterase

b. Inhibition of MAO

97
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[HEAVY METALS]

Types of Hg

a. Elemental Hg

b. Inorganic Hg

c. Organic Hg

a. HgCl2 (corrosive sublimate) = _____

b. amalgam = _____

c. methyl mercury = _____

d. thermometers = _____

e. Hg2Cl2 (calomel) = _____

f. thimerosal (Merthiolate) = _____

a. HgCl2 (corrosive sublimate) = Inorganic Hg

b. amalgam = Elemental Hg

c. methyl mercury = Organic Hg

d. thermometers = Elemental Hg

e. Hg2Cl2 (calomel) = Inorganic Hg

f. thimerosal (Merthiolate) = Organic Hg

98
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[HEAVY METALS]

Mercury poisoning in children may cause:

a. Pink disease (Acrodynia)
b. Gray baby syndrome
c. Reye syndrome
d. Stevens-Johnson syndrome

a. Pink disease (Acrodynia)

99
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[HEAVY METALS]

Which findings are characteristics of Acrodynia?

a. Blue gums
b. Pink palms and soles
c. Jaundice
d. Photophobia

b. Pink palms and soles &

d. Photophobia

100
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[HEAVY METALS]

The triad of Mad Hatter's disease includes all EXCEPT:

a. Erethism (Neuropsychiatric disorder)
b. Gingivostomatitis
c. Tremor
d. Saturnism

d. Saturnism