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All are features of Abetalipoproteinemia, EXCEPT:

Plasma levels of cholesterol and triglyceride are extremely low

Manifest in early childhood with diarrhea

Progressive pigmented retinopathy seen

Neurological manifestation as ataxia in first decade

Question: All are features of Abetalipoproteinemia, EXCEPT: Choices: A. Plasma levels of cholesterol and triglyceride are extremely low B. Manifest in early childhood with diarrhea C. Progressive pigmented retinopathy seen D. Neurological manifestation as ataxia in first decade Answer:

Abetalipoproteinemia is due to deficiency of -

Lecithin Cholesterol Acyl Transferase

ATP Binding Cassette Transporter-1

Mitochondrial Triglyceride Transfer Protein

ApoCII

Question: Abetalipoproteinemia is due to deficiency of - Choices: A. Lecithin Cholesterol Acyl Transferase B. ATP Binding Cassette Transporter-1 C. Mitochondrial Triglyceride Transfer Protein D. ApoCII Answer:

Small intestinal biopsy is diagnostic in :a) Whipple's diseaseb) Abetalipoproteinemiac) Celiac diseased) Agammaglobulinemia

acd

bcd

abd

ab

Question: Small intestinal biopsy is diagnostic in :a) Whipple's diseaseb) Abetalipoproteinemiac) Celiac diseased) Agammaglobulinemia Choices: A. acd B. bcd C. abd D. ab Answer:

Intermittent dysphagia is caused by -a) Strictureb) Reflux esophagitisc) Achalasia cardiad) Pharyngeal diverticululame) Diffuse esophageal spasm

ab

bc

de

bd

Question: Intermittent dysphagia is caused by -a) Strictureb) Reflux esophagitisc) Achalasia cardiad) Pharyngeal diverticululame) Diffuse esophageal spasm Choices: A. ab B. bc C. de D. bd Answer:

Following are radiological evidence of Achalasia cardia except not related -radiology

Smooth narrowing of esophagus

Dilated touous esophagus

Absence of air in the fundus

Exaggerated peristalsis

Question: Following are radiological evidence of Achalasia cardia except not related -radiology Choices: A. Smooth narrowing of esophagus B. Dilated touous esophagus C. Absence of air in the fundus D. Exaggerated peristalsis Answer:

Which drug is used for Achalasia cardia-

Nifedipine

Propranolal

Atenolol

Bethnecol

Question: Which drug is used for Achalasia cardia- Choices: A. Nifedipine B. Propranolal C. Atenolol D. Bethnecol Answer:

Achalasia is associated with increased risk of ...... malignancy:

Squamous cell carcinoma esophagus

Adenocarcinoma esophagus

Bronchogenic carcinoma

Bronchial adenoma

Question: Achalasia is associated with increased risk of ...... malignancy: Choices: A. Squamous cell carcinoma esophagus B. Adenocarcinoma esophagus C. Bronchogenic carcinoma D. Bronchial adenoma Answer:

Which investigation is not required in diagnosis of Achalasia?

Esophageal manometry

Barium swallow

Anti-neuronal antibodies

Enterocylsis

Question: Which investigation is not required in diagnosis of Achalasia? Choices: A. Esophageal manometry B. Barium swallow C. Anti-neuronal antibodies D. Enterocylsis Answer:

About Achalasia Cardia: 1. Dysphagia is a presenting symptom 2. The cause is the absence of Auerbach's plexus 3. Esophagectomy is the treatment 4. Motility improving agents are used in treatment 5. Barium swallow shows irregular filling defects in lower esophagus

1,2,3 False & 4,5 True

1,2,4 True & 3,5 False

2,3,4 True &1,5 False

1,3,5 True & 2,4 False

Question: About Achalasia Cardia: 1. Dysphagia is a presenting symptom 2. The cause is the absence of Auerbach's plexus 3. Esophagectomy is the treatment 4. Motility improving agents are used in treatment 5. Barium swallow shows irregular filling defects in lower esophagus Choices: A. 1,2,3 False & 4,5 True B. 1,2,4 True & 3,5 False C. 2,3,4 True &1,5 False D. 1,3,5 True & 2,4 False Answer:

Feature of Achalasia cardia (cardiospasm) include all of the following except-

Increasing dificulty in swallowing more for liquids than for soilds

Regurgitant vomiting

Dilated & turtuous esophagus

Filling defect on barium study

Question: Feature of Achalasia cardia (cardiospasm) include all of the following except- Choices: A. Increasing dificulty in swallowing more for liquids than for soilds B. Regurgitant vomiting C. Dilated & turtuous esophagus D. Filling defect on barium study Answer:

Barret's esophagus can lead to -a) Strictureb) Reflux esophagitisc) Peptic ulcerd) Achalasia

ac

bc

ad

b

Question: Barret's esophagus can lead to -a) Strictureb) Reflux esophagitisc) Peptic ulcerd) Achalasia Choices: A. ac B. bc C. ad D. b Answer:

Odynophagia occurs ina) Achalasiab) Herpes esophagitisc) Monilial esophagitisd) Barret's oesophagus

a

c

ac

bc

Question: Odynophagia occurs ina) Achalasiab) Herpes esophagitisc) Monilial esophagitisd) Barret's oesophagus Choices: A. a B. c C. ac D. bc Answer:

Achalasia cardia presents with all EXCEPT:

Increased lower esophalgus sphincter tone

Normal peristalsis

Dilatation proximally

Malignancy

Question: Achalasia cardia presents with all EXCEPT: Choices: A. Increased lower esophalgus sphincter tone B. Normal peristalsis C. Dilatation proximally D. Malignancy Answer:

Intermittent dysphagia is caused by -a) Strictureb) Reflux esophagitisc) Achalasia cardiad) Pharyngeal diverticulme) Diffuse esophageal spasm

ab

bc

cd

de

Question: Intermittent dysphagia is caused by -a) Strictureb) Reflux esophagitisc) Achalasia cardiad) Pharyngeal diverticulme) Diffuse esophageal spasm Choices: A. ab B. bc C. cd D. de Answer:

Radiologic feature suggestive of Achalasia cardia is?

Absence of gastric air bubble

Air fluid level in mediastinum

Sigmoid ecophagus

All of the above

Question: Radiologic feature suggestive of Achalasia cardia is? Choices: A. Absence of gastric air bubble B. Air fluid level in mediastinum C. Sigmoid ecophagus D. All of the above Answer:

Achalasia cardia due to:

Degeneration of myenteric plexus due to toxin

Degeneration and absence of ganglion cells in auerbach' Plexus

Excess of Ganglion cells in auerbach Plexus

Degeneration of meissner's Plexus

Question: Achalasia cardia due to: Choices: A. Degeneration of myenteric plexus due to toxin B. Degeneration and absence of ganglion cells in auerbach' Plexus C. Excess of Ganglion cells in auerbach Plexus D. Degeneration of meissner's Plexus Answer:

In which of the following condition does odynohagia occur? 1. Achalasia 2. Herpes esophagitis 3. Monilial esophagitis 4. Barrett's esophagus

1 & 2

2 & 3

1,2 & 3

1,2,3 & 4

Question: In which of the following condition does odynohagia occur? 1. Achalasia 2. Herpes esophagitis 3. Monilial esophagitis 4. Barrett's esophagus Choices: A. 1 & 2 B. 2 & 3 C. 1,2 & 3 D. 1,2,3 & 4 Answer:

Following are radiological evidence of Achalasia cardia Except

Beak like appearance

Dilated touous esophagus

Presence of air-fluid level

Exaggerated peristalsis

Question: Following are radiological evidence of Achalasia cardia Except Choices: A. Beak like appearance B. Dilated touous esophagus C. Presence of air-fluid level D. Exaggerated peristalsis Answer:

Which of the following disease causes Achalasia

Kala azar

Chaga's disease

KFD

Schistosomiasis

Question: Which of the following disease causes Achalasia Choices: A. Kala azar B. Chaga's disease C. KFD D. Schistosomiasis Answer:

In which of the following conditions, uniform dilation of esophagus is seen -a) Sclerodermab) Achalasia cardiac) Dermatomyositisd) Trypanosoma cruzi infection

c

bd

ab

ac

Question: In which of the following conditions, uniform dilation of esophagus is seen -a) Sclerodermab) Achalasia cardiac) Dermatomyositisd) Trypanosoma cruzi infection Choices: A. c B. bd C. ab D. ac Answer:

Radiologic feature suggestive of Achalasia cardia is-

Absence of gastric air bubble

Air fluid level in mediastinum

Sigmoid ecophagus

All of the above

Question: Radiologic feature suggestive of Achalasia cardia is- Choices: A. Absence of gastric air bubble B. Air fluid level in mediastinum C. Sigmoid ecophagus D. All of the above Answer:

Intermittent dysphagia is caused by? 1. Stricture 2. Reflux esophagitis 3. Achalasia cardia 4. Pharyngeal diveiculum 5. Diffuse esophageal spasm

1,2 & 3

2,3 & 4

4 & 5

3,4 & 5

Question: Intermittent dysphagia is caused by? 1. Stricture 2. Reflux esophagitis 3. Achalasia cardia 4. Pharyngeal diveiculum 5. Diffuse esophageal spasm Choices: A. 1,2 & 3 B. 2,3 & 4 C. 4 & 5 D. 3,4 & 5 Answer:

Gold standard Investigation for Achalasia cardia is :

Esophageal manometry

Barium swallow

Endoscopy

Endoscopic ultrasound

Question: Gold standard Investigation for Achalasia cardia is : Choices: A. Esophageal manometry B. Barium swallow C. Endoscopy D. Endoscopic ultrasound Answer:

Achalasia cardia

Absence of nerves

Absence of muscles

Hyperophy of nerves

Hyperophy of muscles

Question: Achalasia cardia Choices: A. Absence of nerves B. Absence of muscles C. Hyperophy of nerves D. Hyperophy of muscles Answer:

Mode of inheritance forAchondroplasia is -

Autosomal dominant

Autosomal recessive

X-linked dominant

X- linked recessive

Question: Mode of inheritance forAchondroplasia is - Choices: A. Autosomal dominant B. Autosomal recessive C. X-linked dominant D. X- linked recessive Answer:

The features of Achondroplasia inlcude all,except -a) Defective headb) Mental retardationc) Autosomal recessived) Familial

bc

c

ac

ad

Question: The features of Achondroplasia inlcude all,except -a) Defective headb) Mental retardationc) Autosomal recessived) Familial Choices: A. bc B. c C. ac D. ad Answer:

Most common inheritance of Achondroplasia is

Sporadic

Autosomal dominant

Autosomal recessive

X-linked recessive

Question: Most common inheritance of Achondroplasia is Choices: A. Sporadic B. Autosomal dominant C. Autosomal recessive D. X-linked recessive Answer:

Achondroplasia shows which of the following type of inheritance

Autosomal Dominant

Autosomal Recessive

X-Linked Dominant

X-Linked Recessive

Question: Achondroplasia shows which of the following type of inheritance Choices: A. Autosomal Dominant B. Autosomal Recessive C. X-Linked Dominant D. X-Linked Recessive Answer:

All of the following are features of Achondroplasia except:

Bullet shaped veebra

Trident hand/starfish hand

Wimberger ring sign

Champagne glass pelvis

Question: All of the following are features of Achondroplasia except: Choices: A. Bullet shaped veebra B. Trident hand/starfish hand C. Wimberger ring sign D. Champagne glass pelvis Answer:

Microcephaly is seen in Beckwith hypoglycaemic syndrome Fanconi syndrome Down syndrome Achondroplasia

I and iv

I and ii

ii and iii

ii and iv

Question: Microcephaly is seen in Beckwith hypoglycaemic syndrome Fanconi syndrome Down syndrome Achondroplasia Choices: A. I and iv B. I and ii C. ii and iii D. ii and iv Answer:

True statement regarding Achondroplasia is :

AR inheritance

Shortened spine

Increased risk of pathological fracture

Diagnosed at birth by X-ray

Question: True statement regarding Achondroplasia is : Choices: A. AR inheritance B. Shortened spine C. Increased risk of pathological fracture D. Diagnosed at birth by X-ray Answer:

If both husband and wife are suffering with Achondroplasia, what are their chances of having a normal child?

0%

25%

50%

100%

Question: If both husband and wife are suffering with Achondroplasia, what are their chances of having a normal child? Choices: A. 0% B. 25% C. 50% D. 100% Answer:

All are true about Achondroplasia except

Antosomal dominant

Acral osteolysis

Trident hand

Champaigne glass pelvis

Question: All are true about Achondroplasia except Choices: A. Antosomal dominant B. Acral osteolysis C. Trident hand D. Champaigne glass pelvis Answer:

Not a feature of Achondroplasia

Tombstone iliac bone

Champagne glass pelvis

Acromelic dwarfism

Bullet shaped veebra

Question: Not a feature of Achondroplasia Choices: A. Tombstone iliac bone B. Champagne glass pelvis C. Acromelic dwarfism D. Bullet shaped veebra Answer:

Achondroplasia shows which of the following type of inheritance?

Autosomal dominant

Autosomal recessive

X linked dominant

X linked recessive

Question: Achondroplasia shows which of the following type of inheritance? Choices: A. Autosomal dominant B. Autosomal recessive C. X linked dominant D. X linked recessive Answer:

The earliest Cranial nerve involved in Acoustic Neuroma is:

V

VI

VII

X

Question: The earliest Cranial nerve involved in Acoustic Neuroma is: Choices: A. V B. VI C. VII D. X Answer:

Acromegaly is due to excess of:

Somatomedin

Growth hormone

Somatostation

Insulin

Question: Acromegaly is due to excess of: Choices: A. Somatomedin B. Growth hormone C. Somatostation D. Insulin Answer:

Deficiency of growth hormone leads to –a) Delayed fusion of epiphysisb) Proportionate dwarfismc) Acromegaly d) Mental retardation

ac

a

ab

bc

Question: Deficiency of growth hormone leads to –a) Delayed fusion of epiphysisb) Proportionate dwarfismc) Acromegaly d) Mental retardation Choices: A. ac B. a C. ab D. bc Answer:

Acromegaly is associated with all of the following EXCEPT:

Nasal sinus enlargement

Increased heel pad thickness

Diabetes mellitus

Muscle hyperophy

Question: Acromegaly is associated with all of the following EXCEPT: Choices: A. Nasal sinus enlargement B. Increased heel pad thickness C. Diabetes mellitus D. Muscle hyperophy Answer:

Angioid streaks is seen in -a) Pseudoxanthoma Elasticumb) Acromegalyc) Paget's diseased) All of above

a

ac

ad

b

Question: Angioid streaks is seen in -a) Pseudoxanthoma Elasticumb) Acromegalyc) Paget's diseased) All of above Choices: A. a B. ac C. ad D. b Answer:

In Acromegaly All of the following are seen EXCEPT

Visceromegaly

Decreased sweating

Hypertension

Soft tissue and bone enlargement

Question: In Acromegaly All of the following are seen EXCEPT Choices: A. Visceromegaly B. Decreased sweating C. Hypertension D. Soft tissue and bone enlargement Answer:

Confirmatory investigation for Acromegaly is:

Insulin induced GH suppression

Glucose induced GH suppression

Random GH assay

IGF - I level

Question: Confirmatory investigation for Acromegaly is: Choices: A. Insulin induced GH suppression B. Glucose induced GH suppression C. Random GH assay D. IGF - I level Answer:

Acromegaly is a disorder of:

Excess growth hormone secretion during adulthood

Excess thyroxine secretion

Excess ACTH secretion

Excess FSH secretion

Question: Acromegaly is a disorder of: Choices: A. Excess growth hormone secretion during adulthood B. Excess thyroxine secretion C. Excess ACTH secretion D. Excess FSH secretion Answer:

Acromegaly results due to excessive release of:

Thyroxine

Growth hormone

Insulin

Glucagon

Question: Acromegaly results due to excessive release of: Choices: A. Thyroxine B. Growth hormone C. Insulin D. Glucagon Answer:

Acromegaly is associated with

Class. I malocclusion

Class. I cross bite

Class. II malocclusion

Class. III malocclusion

Question: Acromegaly is associated with Choices: A. Class. I malocclusion B. Class. I cross bite C. Class. II malocclusion D. Class. III malocclusion Answer:

Drug used in Acute Intermittent Porphyria is

Opioids

Phenobarbitone

Primidone

Blood tranfusion

Question: Drug used in Acute Intermittent Porphyria is Choices: A. Opioids B. Phenobarbitone C. Primidone D. Blood tranfusion Answer:

All of the following genetic syndromes are associated with Acute Myeloid Leukemia, except:

Down's Syndrome

Klinefelter's Syndrome

Patau Syndrome

Turner's Syndrome

Question: All of the following genetic syndromes are associated with Acute Myeloid Leukemia, except: Choices: A. Down's Syndrome B. Klinefelter's Syndrome C. Patau Syndrome D. Turner's Syndrome Answer:

A child with Acute Myeloid Leukemia presents with hyperleukocytosis. Treatment includes all of the following except ?

IV fluid

Allopurinol

Alkalinization

Immediately sta induction chemotherapy

Question: A child with Acute Myeloid Leukemia presents with hyperleukocytosis. Treatment includes all of the following except ? Choices: A. IV fluid B. Allopurinol C. Alkalinization D. Immediately sta induction chemotherapy Answer:

Which of the following is a poor prognostic factor in Acute Myeloid Leukemia (AML)

Monosomy

Deletion of X or Y chromosome

t (8; 21) translocation

Nucleophosphin mutation

Question: Which of the following is a poor prognostic factor in Acute Myeloid Leukemia (AML) Choices: A. Monosomy B. Deletion of X or Y chromosome C. t (8; 21) translocation D. Nucleophosphin mutation Answer:

Non-specific esterase is positive in all the categories of Acute Myeloid Leukemia, EXCEPT:

M3

M4

M5

M6

Question: Non-specific esterase is positive in all the categories of Acute Myeloid Leukemia, EXCEPT: Choices: A. M3 B. M4 C. M5 D. M6 Answer:

The cause of the severe hemorrhage in Acute Promyelocytic Leukemia is?

Disseminated intravascular coagulation

Immune complex deposits on blood vessels

Thrombocytopenia

Thrombocytosis

Question: The cause of the severe hemorrhage in Acute Promyelocytic Leukemia is? Choices: A. Disseminated intravascular coagulation B. Immune complex deposits on blood vessels C. Thrombocytopenia D. Thrombocytosis Answer:

A 26 year old man is critically ill, with multisystem organ failure, and he has not been able to give a clear history of respiratory distress. You suspect Acute Respiratory Distress Syndrome (ARDS). 1. The lung injury may be direct, as occurs in sepsis, or indirect, as occurs in Toxic inhalation 2. The aerial (a) PO2 (in mmHg)/FIO2 (inspiratory O2 fraction) > 200 mmHg is characteristic of ARDS 3. Ventilator-induced injury will be more with low tidal volume ventilation in ARDS 4. Moality was significantly lower in the high tidal volume ventilation, compared to the conventional tidal volume ventilated patients 5. High-dose glucocoicoids are useful in the care of ARDS patients

1,2,5-True & 3,4-False

All True

All False

3,4-True & 1,2,5-False

Question: A 26 year old man is critically ill, with multisystem organ failure, and he has not been able to give a clear history of respiratory distress. You suspect Acute Respiratory Distress Syndrome (ARDS). 1. The lung injury may be direct, as occurs in sepsis, or indirect, as occurs in Toxic inhalation 2. The aerial (a) PO2 (in mmHg)/FIO2 (inspiratory O2 fraction) > 200 mmHg is characteristic of ARDS 3. Ventilator-induced injury will be more with low tidal volume ventilation in ARDS 4. Moality was significantly lower in the high tidal volume ventilation, compared to the conventional tidal volume ventilated patients 5. High-dose glucocoicoids are useful in the care of ARDS patients Choices: A. 1,2,5-True & 3,4-False B. All True C. All False D. 3,4-True & 1,2,5-False Answer:

Diffuse specific lesions on intestinal biopsy are seen in -a) Celiac sprueb) Whipples diseasec) Agammaglobulinemia d) Abetalipoproteinemal

abc

bcd

ac

bd

Question: Diffuse specific lesions on intestinal biopsy are seen in -a) Celiac sprueb) Whipples diseasec) Agammaglobulinemia d) Abetalipoproteinemal Choices: A. abc B. bcd C. ac D. bd Answer:

Agammaglobulinemia can present with?

Rhinitis

Bronchiectasis

Giardia infections

All above

Question: Agammaglobulinemia can present with? Choices: A. Rhinitis B. Bronchiectasis C. Giardia infections D. All above Answer:

Diagnosis of X linked Agammaglobulinemia should be suspected if:

Female sex

Absent tonsils and no palpable lymph nodes on physical examination

High isohemagglutinins titers

Low CD3

Question: Diagnosis of X linked Agammaglobulinemia should be suspected if: Choices: A. Female sex B. Absent tonsils and no palpable lymph nodes on physical examination C. High isohemagglutinins titers D. Low CD3 Answer:

Alkaptonuria an inherited metabolic disorder is due to the deficiency of

Homogentisate oxidase

Cystathionase

Pheylalanine hydroxylase

Tyrosine transaminase

Question: Alkaptonuria an inherited metabolic disorder is due to the deficiency of Choices: A. Homogentisate oxidase B. Cystathionase C. Pheylalanine hydroxylase D. Tyrosine transaminase Answer:

Alkaptonuria is caused by defect in which of the following enzymes?

Enolase

Homogentisate oxidase

Pyruvate carboxylase

None of the above

Question: Alkaptonuria is caused by defect in which of the following enzymes? Choices: A. Enolase B. Homogentisate oxidase C. Pyruvate carboxylase D. None of the above Answer:

Enzyme-deficient in Alkaptonuria

Phenylalanine hydroxylase

Cystathionine synthase

Homogentisic acid oxidase

Tyrosinase

Question: Enzyme-deficient in Alkaptonuria Choices: A. Phenylalanine hydroxylase B. Cystathionine synthase C. Homogentisic acid oxidase D. Tyrosinase Answer:

The earliest manifestation of Alkaptonuria is -

Ankylosis of lumbodorsal spine

Ochronotic arthritis

Prostatic calculi

Pigmentation of tympanic membrane

Question: The earliest manifestation of Alkaptonuria is - Choices: A. Ankylosis of lumbodorsal spine B. Ochronotic arthritis C. Prostatic calculi D. Pigmentation of tympanic membrane Answer:

Enzyme deficient in Alkaptonuria?

Phenylalanine hydroxylase

Cystathionine synthase

Homogentisic acid oxidase

Tyrosinase

Question: Enzyme deficient in Alkaptonuria? Choices: A. Phenylalanine hydroxylase B. Cystathionine synthase C. Homogentisic acid oxidase D. Tyrosinase Answer:

Which of the following is used to treat Alkaptonuria?

Vitamin A

Vitamin C

Vitamin D

Vitamin K

Question: Which of the following is used to treat Alkaptonuria? Choices: A. Vitamin A B. Vitamin C C. Vitamin D D. Vitamin K Answer:

Which substance gets accumulated in abnormal amounts in Alkaptonuria

Acetoacetate

Oxalate

Homogentisate

Phenylacetic acid

Question: Which substance gets accumulated in abnormal amounts in Alkaptonuria Choices: A. Acetoacetate B. Oxalate C. Homogentisate D. Phenylacetic acid Answer:

Which is false about Alkaptonuria?

Genitourinary system not involved

Hemogentistic oxidase deficiency

Black urine

Calcification in veebral bodies

Question: Which is false about Alkaptonuria? Choices: A. Genitourinary system not involved B. Hemogentistic oxidase deficiency C. Black urine D. Calcification in veebral bodies Answer:

Treatment of Alkaptonuria:

Vitamin A

Vitamin C

Vitamin D

Vitamin K

Question: Treatment of Alkaptonuria: Choices: A. Vitamin A B. Vitamin C C. Vitamin D D. Vitamin K Answer:

Enzyme deficiency in Alkaptonuria is

Tyrosine hydroxylase

Homogentisate acid oxidase

Phenyl alanine hydroxylase

Cystathione synthase

Question: Enzyme deficiency in Alkaptonuria is Choices: A. Tyrosine hydroxylase B. Homogentisate acid oxidase C. Phenyl alanine hydroxylase D. Cystathione synthase Answer:

In Alkaptonuria deficiency is:

Phosphofructo kinase

HMG CoA reductase

Homogentisate oxidase

Xanthine oxidase

Question: In Alkaptonuria deficiency is: Choices: A. Phosphofructo kinase B. HMG CoA reductase C. Homogentisate oxidase D. Xanthine oxidase Answer:

Alkaptonuria is a metabolic disease caused by a defect in or lack of homogentisic acid oxidase which lead to

Absent patella

Blue sclera

Darkly pigmented sclera cornea & ear

Absent radii

Question: Alkaptonuria is a metabolic disease caused by a defect in or lack of homogentisic acid oxidase which lead to Choices: A. Absent patella B. Blue sclera C. Darkly pigmented sclera cornea & ear D. Absent radii Answer:

Calcification of intervertebral disc is seen in – a) Goutb) Rheumatoid c) Alkaptonuriad) Psoriasis

ac

bc

ad

b

Question: Calcification of intervertebral disc is seen in – a) Goutb) Rheumatoid c) Alkaptonuriad) Psoriasis Choices: A. ac B. bc C. ad D. b Answer:

Alkaptonuria is due to deficiency of

Alkaptonase

Tyrosinase

Phenylalanine hydroxylase

Homogentisic acid oxidase

Question: Alkaptonuria is due to deficiency of Choices: A. Alkaptonase B. Tyrosinase C. Phenylalanine hydroxylase D. Homogentisic acid oxidase Answer:

All of the following are used in Alopecia Areata except

Tacrolimus

Acitretin

Steroids

Phototherapy

Question: All of the following are used in Alopecia Areata except Choices: A. Tacrolimus B. Acitretin C. Steroids D. Phototherapy Answer:

Which one of the following is NOT true of Ameloblastoma -

Most common odontogenic tumour

Generally benign

Common in 3rd to 5th decade

Arises from mesenchymal tissue

Question: Which one of the following is NOT true of Ameloblastoma - Choices: A. Most common odontogenic tumour B. Generally benign C. Common in 3rd to 5th decade D. Arises from mesenchymal tissue Answer:

True about Ameloblastoma: (PGI Dec 2006)

Cystic lesion

Rapidly growing

Malignant disease

MC site is Tibia

Question: True about Ameloblastoma: (PGI Dec 2006) Choices: A. Cystic lesion B. Rapidly growing C. Malignant disease D. MC site is Tibia Answer:

Ameloblastoma most frequently occurs in

Mandibular molar region

Maxillary molar region

Mandibular premolar region

Maxillary premolar region

Question: Ameloblastoma most frequently occurs in Choices: A. Mandibular molar region B. Maxillary molar region C. Mandibular premolar region D. Maxillary premolar region Answer:

True about Ameloblastoma -a) Cystic lesionb) Rapidly growingc) Malignant diseased) MC site is Tibiae) Presented in children

ae

b

ab

ad

Question: True about Ameloblastoma -a) Cystic lesionb) Rapidly growingc) Malignant diseased) MC site is Tibiae) Presented in children Choices: A. ae B. b C. ab D. ad Answer:

Congo red staining of abdominal fat has confirmed a diagnosis of Amyloidosis in a 28-year-old man. Which is the most common cause of death in primary AL Amylodosis?

Respiratory failure

Cardiac failure

Renal failure

Septicemia

Question: Congo red staining of abdominal fat has confirmed a diagnosis of Amyloidosis in a 28-year-old man. Which is the most common cause of death in primary AL Amylodosis? Choices: A. Respiratory failure B. Cardiac failure C. Renal failure D. Septicemia Answer:

Amyloidosis of hea presents with -

Arrhythmia

AV block

|Ed mass/voltage

AS

Question: Amyloidosis of hea presents with - Choices: A. Arrhythmia B. AV block C. |Ed mass/voltage D. AS Answer:

Which type of Amyloidosis is caused by mutation of the transthyretin protein ?-

Familial Mediterranean fever

Familial amyloidotic polyneuropathy

Dialysis associated amyloidosis

Prion protein associated amyloidosis

Question: Which type of Amyloidosis is caused by mutation of the transthyretin protein ?- Choices: A. Familial Mediterranean fever B. Familial amyloidotic polyneuropathy C. Dialysis associated amyloidosis D. Prion protein associated amyloidosis Answer:

Amyloidosis is most commonly seen in ?

Maturity onset DM

Type I DM

Type H DM

HTN

Question: Amyloidosis is most commonly seen in ? Choices: A. Maturity onset DM B. Type I DM C. Type H DM D. HTN Answer:

Amyloidosis is commonly associated with:

Chronic osteomyelitis

Periostitis

Acute osteomyelitis

Multiple myeloma

Question: Amyloidosis is commonly associated with: Choices: A. Chronic osteomyelitis B. Periostitis C. Acute osteomyelitis D. Multiple myeloma Answer:

Amyloidosis causes which type of cardiomyopathy?

Constrictive

Restrictive

Hypertrophic

Any of the above

Question: Amyloidosis causes which type of cardiomyopathy? Choices: A. Constrictive B. Restrictive C. Hypertrophic D. Any of the above Answer:

Polyneuropathy is seen in -a) Vitamin deficiencyb) Osteoporosisc) DMd) Myxoedemae) Amyloidosis

bce

acde

abcd

abde

Question: Polyneuropathy is seen in -a) Vitamin deficiencyb) Osteoporosisc) DMd) Myxoedemae) Amyloidosis Choices: A. bce B. acde C. abcd D. abde Answer:

Amyloidosis is seen in which type of diabetes mellitus?

Maturity onset DM

Type I DM

Type II DM

all of the above

Question: Amyloidosis is seen in which type of diabetes mellitus? Choices: A. Maturity onset DM B. Type I DM C. Type II DM D. all of the above Answer:

Small intestinal biopsy is specific for-a) Tropical sprueb) Celiac spruec) Whipple's diseased) Amyloidosis

cd

bc

bd

ac

Question: Small intestinal biopsy is specific for-a) Tropical sprueb) Celiac spruec) Whipple's diseased) Amyloidosis Choices: A. cd B. bc C. bd D. ac Answer:

Amyloidosis mostly affects

Liver

Tounge

Colon

Hea

Question: Amyloidosis mostly affects Choices: A. Liver B. Tounge C. Colon D. Hea Answer:

Confirmatory test for the diagnosis ofAmyloidosis is?

Diagnostic peritoneal lavage

Tongue biopsy

Rectal biopsy

Whole body CT scan

Question: Confirmatory test for the diagnosis ofAmyloidosis is? Choices: A. Diagnostic peritoneal lavage B. Tongue biopsy C. Rectal biopsy D. Whole body CT scan Answer:

Amyloidosis shown in Cardiac muscle is mainly due to …….. fibril

AL

AA

AANF

ATTR

Question: Amyloidosis shown in Cardiac muscle is mainly due to …….. fibril Choices: A. AL B. AA C. AANF D. ATTR Answer:

Major fibril protein in Primary Amyloidosis is ?

AL

AA

Transthyretin

Procalciton

Question: Major fibril protein in Primary Amyloidosis is ? Choices: A. AL B. AA C. Transthyretin D. Procalciton Answer:

Major fibril protein in Primary Amyloidosis is -

AL

AA

Transthyretin

Procalcitonin

Question: Major fibril protein in Primary Amyloidosis is - Choices: A. AL B. AA C. Transthyretin D. Procalcitonin Answer:

Confirmatory test for the diagnosis of Amyloidosis-

Diagnostic peritoneal lavage

Tongue biopsy

Rectal biopsy

Whole body CT scan

Question: Confirmatory test for the diagnosis of Amyloidosis- Choices: A. Diagnostic peritoneal lavage B. Tongue biopsy C. Rectal biopsy D. Whole body CT scan Answer:

Confirmatory test for the diagnosis of Amyloidosis is:

Diagnostic peritoneal lavage

Tongue biopsy

Rectal biopsy

Whole body CT scan

Question: Confirmatory test for the diagnosis of Amyloidosis is: Choices: A. Diagnostic peritoneal lavage B. Tongue biopsy C. Rectal biopsy D. Whole body CT scan Answer:

Amyloidosis of heart presents with -a) Arrhythmiab) AV blockc) ↑ed mass/voltage d) Hypertrophic cardiomyopathy

ab

abc

acd

bcd

Question: Amyloidosis of heart presents with -a) Arrhythmiab) AV blockc) ↑ed mass/voltage d) Hypertrophic cardiomyopathy Choices: A. ab B. abc C. acd D. bcd Answer:

Amyloidosis is most commonly seen in-

Maturity onset DM

Type I DM

Type II DM

HTN

Question: Amyloidosis is most commonly seen in- Choices: A. Maturity onset DM B. Type I DM C. Type II DM D. HTN Answer:

Which type ofAmyloidosis is caused by mutation of the transthyretin protein ?

Familial Mediterranean fever

Familial amyloidotic polyneuropathy

Dialysis associated amyloidosis

Prion protein associated amyloidosis

Question: Which type ofAmyloidosis is caused by mutation of the transthyretin protein ? Choices: A. Familial Mediterranean fever B. Familial amyloidotic polyneuropathy C. Dialysis associated amyloidosis D. Prion protein associated amyloidosis Answer:

Amyloidosis is most commonly seen in

Maturity onset DM

Type1DM

Type2DM

Equally seen with all forms of DM

Question: Amyloidosis is most commonly seen in Choices: A. Maturity onset DM B. Type1DM C. Type2DM D. Equally seen with all forms of DM Answer:

Amyloidosis is?

RNA misfolding

DNA repair defect

Mitochondrial defect

Misfolding of protein

Question: Amyloidosis is? Choices: A. RNA misfolding B. DNA repair defect C. Mitochondrial defect D. Misfolding of protein Answer:

Paraneoplastic syndrome not seen in renal cell cancer is?a) Acanthosis nigricansb) Amyloidosisc) Polycythemiad) SLE

b

c

ad

ab

Question: Paraneoplastic syndrome not seen in renal cell cancer is?a) Acanthosis nigricansb) Amyloidosisc) Polycythemiad) SLE Choices: A. b B. c C. ad D. ab Answer:

Bone marrow in Amyloid Lightchain Amyloidosis shows which of the following features?

Bone marrow plasmacytosis

Granulomatous reaction

Fibrosis

Giant cell formation

Question: Bone marrow in Amyloid Lightchain Amyloidosis shows which of the following features? Choices: A. Bone marrow plasmacytosis B. Granulomatous reaction C. Fibrosis D. Giant cell formation Answer:

Amyloidosis deposition most commonly occurs in:

Renal vessels

Knee joints

Skin

Cornea

Question: Amyloidosis deposition most commonly occurs in: Choices: A. Renal vessels B. Knee joints C. Skin D. Cornea Answer:

Amyloidosis most commonly affects -

Liver

Tongue

Colon

Hea

Question: Amyloidosis most commonly affects - Choices: A. Liver B. Tongue C. Colon D. Hea Answer:

Which type of Amyloidosis is caused by the mutation of a transthyretin protein?

Dialysis associated amyloidosis

Familial Mediterranean fever

Familial amyloidotic polyneuropathy

Prion protein associated amyloidosis

Question: Which type of Amyloidosis is caused by the mutation of a transthyretin protein? Choices: A. Dialysis associated amyloidosis B. Familial Mediterranean fever C. Familial amyloidotic polyneuropathy D. Prion protein associated amyloidosis Answer: