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The best way to manage Dermatitis Herpetiformis is ?

Gluten free diet with minerals and vitamins

Dapsone

Acyclovir

Steroids

Question: The best way to manage Dermatitis Herpetiformis is ? Choices: A. Gluten free diet with minerals and vitamins B. Dapsone C. Acyclovir D. Steroids Answer:

Which one of the following is the treatment of choice for Dermatitis Herpetiformis?

Corticosteroids

Dapsone

Methotrexate

Retinoids

Question: Which one of the following is the treatment of choice for Dermatitis Herpetiformis? Choices: A. Corticosteroids B. Dapsone C. Methotrexate D. Retinoids Answer:

Dermatomyositis test of choice -

CPK

24hr urine creat

SGOT

SGPT

Question: Dermatomyositis test of choice - Choices: A. CPK B. 24hr urine creat C. SGOT D. SGPT Answer:

True about Dermatomyositis is?

Associated with HLA B27

Bimodal age distribution

No involvement of joints

Myopathy precedes skin lesions in most cases

Question: True about Dermatomyositis is? Choices: A. Associated with HLA B27 B. Bimodal age distribution C. No involvement of joints D. Myopathy precedes skin lesions in most cases Answer:

Common antibody in Polymyositis and Dermatomyositis includes

SS-7

SS-8

Anti-aminoacyl-tRNA synthetase

Anti hystidyl transfer synthetase

Question: Common antibody in Polymyositis and Dermatomyositis includes Choices: A. SS-7 B. SS-8 C. Anti-aminoacyl-tRNA synthetase D. Anti hystidyl transfer synthetase Answer:

All of the following signs are seen in Dermatomyositis except

Heliotrope sign

Gottron sign

Dimple sign

Shawl sign

Question: All of the following signs are seen in Dermatomyositis except Choices: A. Heliotrope sign B. Gottron sign C. Dimple sign D. Shawl sign Answer:

Dracunculosis infection occurs through-

Ingestion of water containing cyclops

Ingestion of water containing the parasite

Ingestion of fish

Penetration of skin

Question: Dracunculosis infection occurs through- Choices: A. Ingestion of water containing cyclops B. Ingestion of water containing the parasite C. Ingestion of fish D. Penetration of skin Answer:

WHO considerations regarding Dracunculosis eradication, all are true except

DDT

Drinking piped water and installation of hand pumps

Health education and awareness of public

Control of Cyclops

Question: WHO considerations regarding Dracunculosis eradication, all are true except Choices: A. DDT B. Drinking piped water and installation of hand pumps C. Health education and awareness of public D. Control of Cyclops Answer:

Dracunculosis is most common in -

Gujarat

Rajasthan

Madhya Pradesh

Orissa

Question: Dracunculosis is most common in - Choices: A. Gujarat B. Rajasthan C. Madhya Pradesh D. Orissa Answer:

Dracunculosis is most common in-

Gujarat

Rajasthan

Madhya Pradesh

Orissa

Question: Dracunculosis is most common in- Choices: A. Gujarat B. Rajasthan C. Madhya Pradesh D. Orissa Answer:

Candidates (s) for global eradication by WHO a. Malariab. Dracunculosis c. Polio d. Measles e. Chicken pox

ab

abd

abc

bcd

Question: Candidates (s) for global eradication by WHO a. Malariab. Dracunculosis c. Polio d. Measles e. Chicken pox Choices: A. ab B. abd C. abc D. bcd Answer:

Dracunculosis infection occurs through?

Ingestion of water containing cyclops

Ingestion of water containing the parasite

Ingestion of fish

Penetration of skin

Question: Dracunculosis infection occurs through? Choices: A. Ingestion of water containing cyclops B. Ingestion of water containing the parasite C. Ingestion of fish D. Penetration of skin Answer:

Dracunculosis infection occurs through -

Ingestion of water containing cyclops

Ingestion of water containing the parasite

Ingestion of fish

Penetration of skin

Question: Dracunculosis infection occurs through - Choices: A. Ingestion of water containing cyclops B. Ingestion of water containing the parasite C. Ingestion of fish D. Penetration of skin Answer:

Duane syndrome involves

Superior oblique

Inferior oblique

Lateral rectus

Superior rectus

Question: Duane syndrome involves Choices: A. Superior oblique B. Inferior oblique C. Lateral rectus D. Superior rectus Answer:

Duchenne Muscular Dystrophy is a disease of:

Neuromuscular junction

Sarcolemmal proteins

Muscle contractile proteins

Disuse atrophy due to muscle weakness

Question: Duchenne Muscular Dystrophy is a disease of: Choices: A. Neuromuscular junction B. Sarcolemmal proteins C. Muscle contractile proteins D. Disuse atrophy due to muscle weakness Answer:

Duchenne Muscular Dystrophy is a disease of-

Neuromuscularj unction

Sarcolemmal proteins

Muscle contractile proteins

Disuse atrophy due to muscle weakness

Question: Duchenne Muscular Dystrophy is a disease of- Choices: A. Neuromuscularj unction B. Sarcolemmal proteins C. Muscle contractile proteins D. Disuse atrophy due to muscle weakness Answer:

Duchenne Muscular Dystrophy is a disease of –

Neuromuscular junction

Sarcolemmal proteins

Muscle contractile proteins

Disuse atrophy due to muscle weakness

Question: Duchenne Muscular Dystrophy is a disease of – Choices: A. Neuromuscular junction B. Sarcolemmal proteins C. Muscle contractile proteins D. Disuse atrophy due to muscle weakness Answer:

Simplex type of Epidermolysis Bullosa involves mutations in

Keratin 5

Lamina lucida

Type vII collagen

Dystrophin

Question: Simplex type of Epidermolysis Bullosa involves mutations in Choices: A. Keratin 5 B. Lamina lucida C. Type vII collagen D. Dystrophin Answer:

Epidermolysis Bullosa simplex is because of defect in:

Collagen 7

Keratin 5 and Keratin 14

Laminin

BP1 and BP2

Question: Epidermolysis Bullosa simplex is because of defect in: Choices: A. Collagen 7 B. Keratin 5 and Keratin 14 C. Laminin D. BP1 and BP2 Answer:

The minimum number of polyps necessary for a diagnosis of Familial Adenomatous Polyposis (FAP) is:

5

10

50

100

Question: The minimum number of polyps necessary for a diagnosis of Familial Adenomatous Polyposis (FAP) is: Choices: A. 5 B. 10 C. 50 D. 100 Answer:

Inheritance of "Familial Hypercholesterolemia" is:

AD

AR

X Linked dominant

X linked recessive

Question: Inheritance of "Familial Hypercholesterolemia" is: Choices: A. AD B. AR C. X Linked dominant D. X linked recessive Answer:

Which of the following is the inheritance pattern of Familial Hypercholesterolemia?

Autosomal dominant

Autosomal recessive

X Linked dominant

X Linked recessive

Question: Which of the following is the inheritance pattern of Familial Hypercholesterolemia? Choices: A. Autosomal dominant B. Autosomal recessive C. X Linked dominant D. X Linked recessive Answer:

Fetal Hydantoin Syndrome is caused by:

Phenytoin

Alcohol

Tetracycline

Sodium valproate

Question: Fetal Hydantoin Syndrome is caused by: Choices: A. Phenytoin B. Alcohol C. Tetracycline D. Sodium valproate Answer:

X-rays findings of "Fibrous Dysplasia" is:

Ground glass density

Calcifications

Coical thickening

Bony expansion

Question: X-rays findings of "Fibrous Dysplasia" is: Choices: A. Ground glass density B. Calcifications C. Coical thickening D. Bony expansion Answer:

X-rays findings of Fibrous Dysplasia is:

Ground glass density

Calcifications

Coical thickening

Bony expansion

Question: X-rays findings of Fibrous Dysplasia is: Choices: A. Ground glass density B. Calcifications C. Coical thickening D. Bony expansion Answer:

In context with Filariasis, all are true except:

Definitive host is man

Worm colonize the lymphatic system

Most common causative agent is W. bancrofti

Transmitted by Aedes aegypti mosquito

Question: In context with Filariasis, all are true except: Choices: A. Definitive host is man B. Worm colonize the lymphatic system C. Most common causative agent is W. bancrofti D. Transmitted by Aedes aegypti mosquito Answer:

Filariasis is cuased due to lymphatic obstruction by -

R vivax

V. bancrofti

C. sinerses

S. hemetabium

Question: Filariasis is cuased due to lymphatic obstruction by - Choices: A. R vivax B. V. bancrofti C. C. sinerses D. S. hemetabium Answer:

Culex mosquito is associated with the transmission of-a) Malariab) Filariasisc) Dengued) Japanese encephalitise) Typhus

c

d

bd

ac

Question: Culex mosquito is associated with the transmission of-a) Malariab) Filariasisc) Dengued) Japanese encephalitise) Typhus Choices: A. c B. d C. bd D. ac Answer:

All of the following are helpful for elimination of Filariasis, except -

Microfilaris do not multiply in vectors

They multiply in humans

Larvae are deposited on skin surface where they can't survive

NOne

Question: All of the following are helpful for elimination of Filariasis, except - Choices: A. Microfilaris do not multiply in vectors B. They multiply in humans C. Larvae are deposited on skin surface where they can't survive D. NOne Answer:

The Clinical incubation period of Filariasis is

10 to 20 days

3 to 6 months

8 to 16 months

6 to 12 months

Question: The Clinical incubation period of Filariasis is Choices: A. 10 to 20 days B. 3 to 6 months C. 8 to 16 months D. 6 to 12 months Answer:

All are true regarding Lymphatic Filariasis except

Causative agent - Wuchereria bancrofti

Intermediate host - Man

Main vector in India - Culex quinquefasciatus

Most common epidemiological method for detection - thick film preparation

Question: All are true regarding Lymphatic Filariasis except Choices: A. Causative agent - Wuchereria bancrofti B. Intermediate host - Man C. Main vector in India - Culex quinquefasciatus D. Most common epidemiological method for detection - thick film preparation Answer:

Filariasis involves

Only superficial lymphatics

Only deep lymphatics

Both superficial and deep lymphatics

Only skin

Question: Filariasis involves Choices: A. Only superficial lymphatics B. Only deep lymphatics C. Both superficial and deep lymphatics D. Only skin Answer:

Treatment for Filariasis is,

Chloroquin

Diethyl Carbamazine

Tetracycline

Praziquantel

Question: Treatment for Filariasis is, Choices: A. Chloroquin B. Diethyl Carbamazine C. Tetracycline D. Praziquantel Answer:

Fox Fordyce Disease effects:

Sebaceous glands

Eccrine Glands

Apocrine glands

Any gland

Question: Fox Fordyce Disease effects: Choices: A. Sebaceous glands B. Eccrine Glands C. Apocrine glands D. Any gland Answer:

Classic Galactosemia is due to deficiency of:

Hexosaminidase

Glucocerebroside

Sphingomyelinase

Galactose-1-Phosphate-Uridyl-Transferase

Question: Classic Galactosemia is due to deficiency of: Choices: A. Hexosaminidase B. Glucocerebroside C. Sphingomyelinase D. Galactose-1-Phosphate-Uridyl-Transferase Answer:

The MOST common enzyme deficiency responsible for Galactosemia is related to which of the following enzymes?

UDP galactose epimerase

Galactokinase

Galactosidase

Galactose-l-phosphate uridyl transferase

Question: The MOST common enzyme deficiency responsible for Galactosemia is related to which of the following enzymes? Choices: A. UDP galactose epimerase B. Galactokinase C. Galactosidase D. Galactose-l-phosphate uridyl transferase Answer:

What is the type of Galactosemia cataract?

Snowflake

Oil drop

Blue dot

Polychromaticlustre

Question: What is the type of Galactosemia cataract? Choices: A. Snowflake B. Oil drop C. Blue dot D. Polychromaticlustre Answer:

Galactosemia is due to deficiency of the following enzymes

Galactose-1-phosphate uridyl transferase

HGPRT

Galactokinase

Epimerase

Question: Galactosemia is due to deficiency of the following enzymes Choices: A. Galactose-1-phosphate uridyl transferase B. HGPRT C. Galactokinase D. Epimerase Answer:

Galactosemia is due to the deficiency of:

Galactose-1-Phosphatase

Glucose-1-Phosphatase

Galcatose-1-Phosphate uridyl transferase

Glucose-6-Phosphatase

Question: Galactosemia is due to the deficiency of: Choices: A. Galactose-1-Phosphatase B. Glucose-1-Phosphatase C. Galcatose-1-Phosphate uridyl transferase D. Glucose-6-Phosphatase Answer:

The enzyme deficient in Galactosemia is:-

Sphingomyelinase

Hexosaminidase

Galactose 1- phosphate uridyl transferase

Glucocerebrosidase

Question: The enzyme deficient in Galactosemia is:- Choices: A. Sphingomyelinase B. Hexosaminidase C. Galactose 1- phosphate uridyl transferase D. Glucocerebrosidase Answer:

The enzyme deficient in Galactosemia is:

Hexoseaminidase B

Hexosaminidase A

Galactose 1 phosphate uridyltransferase

Glucocerebrosidase

Question: The enzyme deficient in Galactosemia is: Choices: A. Hexoseaminidase B B. Hexosaminidase A C. Galactose 1 phosphate uridyltransferase D. Glucocerebrosidase Answer:

Most common enzyme deficiency responsible for Galactosemia is?

UDP galactose epimerase

Galaktokinase

Galactosidase

Galactose-l-phosphate uridyl transferase

Question: Most common enzyme deficiency responsible for Galactosemia is? Choices: A. UDP galactose epimerase B. Galaktokinase C. Galactosidase D. Galactose-l-phosphate uridyl transferase Answer:

Galactosemia commonly is due to deficiency of

Galactose-1 phosphate uridyl transferase

Galactose-1 phosphatase

Glucose-1 phosphatase

Glucose-6 phosphatase

Question: Galactosemia commonly is due to deficiency of Choices: A. Galactose-1 phosphate uridyl transferase B. Galactose-1 phosphatase C. Glucose-1 phosphatase D. Glucose-6 phosphatase Answer:

Galactosemia enzyme defect:

Fructokinase

Glucokinase

Galactose 1 Phosphate Uridyl transferase

Glucose 6 Phosphatase

Question: Galactosemia enzyme defect: Choices: A. Fructokinase B. Glucokinase C. Galactose 1 Phosphate Uridyl transferase D. Glucose 6 Phosphatase Answer:

All of the following are true about Galactosemia EXCEPT?

Galactose 1 phosphate and galactitol have toxic effects on various organs

Patients are symptomatic immediately after bih

Jaundice and liver dysfunction commonly seen

E.coli sepsis is an impoant cause of moality

Question: All of the following are true about Galactosemia EXCEPT? Choices: A. Galactose 1 phosphate and galactitol have toxic effects on various organs B. Patients are symptomatic immediately after bih C. Jaundice and liver dysfunction commonly seen D. E.coli sepsis is an impoant cause of moality Answer:

All of the following tests can help in the diagnosis of Galactosemia EXCEPT?

GALT assay

Mutation analysis

Benedicts test

Guthrie's test

Question: All of the following tests can help in the diagnosis of Galactosemia EXCEPT? Choices: A. GALT assay B. Mutation analysis C. Benedicts test D. Guthrie's test Answer:

Intrahepatic cholestasis is seen in – a) Galactosemiab) Hypercalcemiac) Haemoclu–omatosisd) Cystic fibrosis

ad

c

ac

ab

Question: Intrahepatic cholestasis is seen in – a) Galactosemiab) Hypercalcemiac) Haemoclu–omatosisd) Cystic fibrosis Choices: A. ad B. c C. ac D. ab Answer:

Enzyme deficiency in Galactosemia:

Galactose 1 phosphate uridyl transferase

Aldolase B

UDP galactose 4 epimerase

Fructokinase

Question: Enzyme deficiency in Galactosemia: Choices: A. Galactose 1 phosphate uridyl transferase B. Aldolase B C. UDP galactose 4 epimerase D. Fructokinase Answer:

Which of the following agents is recommended for treatment of Gastrointestinal Stromal Tumors (GIST) -

Sorafenib

Imatinib

Gefitinib

Erlotinib

Question: Which of the following agents is recommended for treatment of Gastrointestinal Stromal Tumors (GIST) - Choices: A. Sorafenib B. Imatinib C. Gefitinib D. Erlotinib Answer:

What is false regarding Gastroschisis & omphalocele:

Intestinal obstruction is common in gastroschisis

Gastroschisis is associated with multiple anamolies

Umbilical cord is attached in normal position in gastroschisis

Liver is the content of omphalocele

Question: What is false regarding Gastroschisis & omphalocele: Choices: A. Intestinal obstruction is common in gastroschisis B. Gastroschisis is associated with multiple anamolies C. Umbilical cord is attached in normal position in gastroschisis D. Liver is the content of omphalocele Answer:

Gastroschisis is associated with :

Younger maternal age

Maternal obesity

Elderly primi

Anaemia

Question: Gastroschisis is associated with : Choices: A. Younger maternal age B. Maternal obesity C. Elderly primi D. Anaemia Answer:

Regarding Gastroschisis and omphalocele which of the following statement is false?

Intestinal obstruction is common in Gastroschisis

Liver is content of Omphalocele

Gastroschisis is associated with multiple anomalies

Umbilical cord is attached in normal position in Omphalocele

Question: Regarding Gastroschisis and omphalocele which of the following statement is false? Choices: A. Intestinal obstruction is common in Gastroschisis B. Liver is content of Omphalocele C. Gastroschisis is associated with multiple anomalies D. Umbilical cord is attached in normal position in Omphalocele Answer:

TRUE about Gestational Trophoblastic Disease is?

Most common site of metastasis is vagina

Presence of Lung metastasis classifies as stage 4 GTN

Liver metastasis carries a poor prognosis similar to brain metastasis

GTN following a term pregnancy has a better prognosis than that with previous molar pregnancy

Question: TRUE about Gestational Trophoblastic Disease is? Choices: A. Most common site of metastasis is vagina B. Presence of Lung metastasis classifies as stage 4 GTN C. Liver metastasis carries a poor prognosis similar to brain metastasis D. GTN following a term pregnancy has a better prognosis than that with previous molar pregnancy Answer:

The highest incidence of Gestational Trophoblastic Disease is in :

Australia

Asia

Noh America

Western Europe

Question: The highest incidence of Gestational Trophoblastic Disease is in : Choices: A. Australia B. Asia C. Noh America D. Western Europe Answer:

Prognosis of Gestational Trophoblastic Disease depends on all, except :

Number of living children

Blood group

Parity

Previous HCG titre

Question: Prognosis of Gestational Trophoblastic Disease depends on all, except : Choices: A. Number of living children B. Blood group C. Parity D. Previous HCG titre Answer:

Glioblastoma multiforme may occur in the following except -

Cerebrum of adult

Brain stem of child

Spinal cord of adult

Adrenal medulla of child

Question: Glioblastoma multiforme may occur in the following except - Choices: A. Cerebrum of adult B. Brain stem of child C. Spinal cord of adult D. Adrenal medulla of child Answer:

Glioblastoma multiforme may occur in the following except:

Cerebrum of adult

Brain stem of child

Spinal cord of adult

Adrenal medulla of child

Question: Glioblastoma multiforme may occur in the following except: Choices: A. Cerebrum of adult B. Brain stem of child C. Spinal cord of adult D. Adrenal medulla of child Answer:

Which of the following is not true about Glioblastoma..

Also known as Butterfly tumor

Frontal lobe of the brain is common location

It belongs to WHO grade 3 Astrocytoma

Serpentine necrosis and glomeruloid bodies

Question: Which of the following is not true about Glioblastoma.. Choices: A. Also known as Butterfly tumor B. Frontal lobe of the brain is common location C. It belongs to WHO grade 3 Astrocytoma D. Serpentine necrosis and glomeruloid bodies Answer:

Which of the following are orbital tumours a) Glioma b) Lymphoma c) Chloroma d) Meningioma e) Schwannoma

abcde

abd

abc

acd

Question: Which of the following are orbital tumours a) Glioma b) Lymphoma c) Chloroma d) Meningioma e) Schwannoma Choices: A. abcde B. abd C. abc D. acd Answer:

Glioma of optic nerve is associated with ?

Neurofibromatosis type I

Neurofibromatosis type II

Both the above

None of the above

Question: Glioma of optic nerve is associated with ? Choices: A. Neurofibromatosis type I B. Neurofibromatosis type II C. Both the above D. None of the above Answer:

Glioma of the optic nerve is usually –

Gemistocytic

Pilocytic

Fibrillary

Lamellar

Question: Glioma of the optic nerve is usually – Choices: A. Gemistocytic B. Pilocytic C. Fibrillary D. Lamellar Answer:

Receptor on neural membrane that induces development of Glioma-

CD133

CD33

CD48

CD44

Question: Receptor on neural membrane that induces development of Glioma- Choices: A. CD133 B. CD33 C. CD48 D. CD44 Answer:

Glioma of the optic nerve is associated with -

Neurofibromatosis type 1

Neurofibromatosis type II

Both the above

None of the above

Question: Glioma of the optic nerve is associated with - Choices: A. Neurofibromatosis type 1 B. Neurofibromatosis type II C. Both the above D. None of the above Answer:

All of the following are features of Hemophagocytic Lymphohistiocytosis (HLH), except:

Fever

Splenomegaly

Hyperferritinemia

Hyperfibrinogenemia

Question: All of the following are features of Hemophagocytic Lymphohistiocytosis (HLH), except: Choices: A. Fever B. Splenomegaly C. Hyperferritinemia D. Hyperfibrinogenemia Answer:

Patients with 'Hemophilia A' have bleeding disorder because of -

Lack of platelet aggregation

Lack of reaction accelerator during activation of factor X in coagulation cascade

Neutralization of antithrombin III

Release of Thromboxane A2

Question: Patients with 'Hemophilia A' have bleeding disorder because of - Choices: A. Lack of platelet aggregation B. Lack of reaction accelerator during activation of factor X in coagulation cascade C. Neutralization of antithrombin III D. Release of Thromboxane A2 Answer:

Hemophilia A due to deficiency of

Factor VIII

Factor IX

Factor X

Factr XI

Question: Hemophilia A due to deficiency of Choices: A. Factor VIII B. Factor IX C. Factor X D. Factr XI Answer:

Which of the following true regarding Hemophilia A

Serum levels of factor VIII are decreased

Deficiency of factor IX

PT increased

FIT decreased

Question: Which of the following true regarding Hemophilia A Choices: A. Serum levels of factor VIII are decreased B. Deficiency of factor IX C. PT increased D. FIT decreased Answer:

Hemophilia A has following except -

↓ VIII factor

↑PTT

↑PT

Normal BT

Question: Hemophilia A has following except - Choices: A. ↓ VIII factor B. ↑PTT C. ↑PT D. Normal BT Answer:

Bleeding disorder with ↑ a PTT is/are -a) Hemophilia Ab) Hemophilia Bc) Henoch-schonlein purpurad) Bernard-soulier syndromee) Von-Willebrand disease

abe

bcd

cde

acd

Question: Bleeding disorder with ↑ a PTT is/are -a) Hemophilia Ab) Hemophilia Bc) Henoch-schonlein purpurad) Bernard-soulier syndromee) Von-Willebrand disease Choices: A. abe B. bcd C. cde D. acd Answer:

Hemophilia A results due to deficiency of which of the factors:

II

VII

VIII

XI

Question: Hemophilia A results due to deficiency of which of the factors: Choices: A. II B. VII C. VIII D. XI Answer:

Which of the following is a recently approved monoclonal antibody for treatment of Hemophilia A?

Emicizumab

Sarilumab

Abaloparatide

Durvalumab

Question: Which of the following is a recently approved monoclonal antibody for treatment of Hemophilia A? Choices: A. Emicizumab B. Sarilumab C. Abaloparatide D. Durvalumab Answer:

Type of DCIS Which of the following true regarding Hemophilia A?

Serum levels of factor VIII are decreased

Deficiency of factor IX

PT increased

PPT decreased

Question: Type of DCIS Which of the following true regarding Hemophilia A? Choices: A. Serum levels of factor VIII are decreased B. Deficiency of factor IX C. PT increased D. PPT decreased Answer:

Hemophilia A is caused due to deficiency of

Factor X

Factor XI

Factor IX

Factor VIII

Question: Hemophilia A is caused due to deficiency of Choices: A. Factor X B. Factor XI C. Factor IX D. Factor VIII Answer:

The most common manifestation of moderate /severe Hemophilia A is:

Recurrent Hemahrosis

Recurrent muscle bleeding

Recurrent bleeding from gums

Recurrent Hematuria

Question: The most common manifestation of moderate /severe Hemophilia A is: Choices: A. Recurrent Hemahrosis B. Recurrent muscle bleeding C. Recurrent bleeding from gums D. Recurrent Hematuria Answer:

Hemophilia A has increased:

PT

PTT

PT & PTT

None

Question: Hemophilia A has increased: Choices: A. PT B. PTT C. PT & PTT D. None Answer:

Hemophilia B is deficiency of which factor:September 2007

IX

XII

VIII

X

Question: Hemophilia B is deficiency of which factor:September 2007 Choices: A. IX B. XII C. VIII D. X Answer:

Hemophilia B is due to deficiency of -

Factor VIII

Factor VII

Factor IX

factor X

Question: Hemophilia B is due to deficiency of - Choices: A. Factor VIII B. Factor VII C. Factor IX D. factor X Answer:

Hemophilia B is due to deficiency of:

Factor VIII

Factor VII

Factor IX

Factor X

Question: Hemophilia B is due to deficiency of: Choices: A. Factor VIII B. Factor VII C. Factor IX D. Factor X Answer:

In Hemophilia B what is most common cause of death?

Hemorrhage

HIV, HBV, HCV due to transfusions

Transfusion reactions

Deep vein thrombosis

Question: In Hemophilia B what is most common cause of death? Choices: A. Hemorrhage B. HIV, HBV, HCV due to transfusions C. Transfusion reactions D. Deep vein thrombosis Answer:

Hemophilia B is due to deficiency of-

Factor VIII

Factor VII

Factor IX

factor X

Question: Hemophilia B is due to deficiency of- Choices: A. Factor VIII B. Factor VII C. Factor IX D. factor X Answer:

Hemophilia B is due to:

Factor VII deficiency

Factor IX deficiency

Platelet deficiency

Vit C deficiency

Question: Hemophilia B is due to: Choices: A. Factor VII deficiency B. Factor IX deficiency C. Platelet deficiency D. Vit C deficiency Answer:

Hemophilia B is deficiency of which factor: September 2007

IX

XII

VIII

X

Question: Hemophilia B is deficiency of which factor: September 2007 Choices: A. IX B. XII C. VIII D. X Answer:

Hepatic Encephalopathy is predisposed by all, Except:

Hyperkalemia

Dehydration

Constipation

GI Bleeding

Question: Hepatic Encephalopathy is predisposed by all, Except: Choices: A. Hyperkalemia B. Dehydration C. Constipation D. GI Bleeding Answer:

Hepatitis D virus (delta agent) is a defective virus that can replicate only in cells already infected with which of the following viruses?

Hepatitis A virus

Epstein-Barr virus

Hepatitis G virus

Hepatitis B virus

Question: Hepatitis D virus (delta agent) is a defective virus that can replicate only in cells already infected with which of the following viruses? Choices: A. Hepatitis A virus B. Epstein-Barr virus C. Hepatitis G virus D. Hepatitis B virus Answer:

Most common mutation in Hereditary Spherocytosis is

Band 3

Ankyrin

Spectrin

Band 4.2

Question: Most common mutation in Hereditary Spherocytosis is Choices: A. Band 3 B. Ankyrin C. Spectrin D. Band 4.2 Answer:

Which of the following is not seen in'Hereditary Spherocytosis:

Direct Coomb's Positive

Increased Osmotic Fragility

Splenomegaly

Gall Stones

Question: Which of the following is not seen in'Hereditary Spherocytosis: Choices: A. Direct Coomb's Positive B. Increased Osmotic Fragility C. Splenomegaly D. Gall Stones Answer:

Which of the following is not seen in Hereditary Spherocytosis

Direct Coomb's Positive

Increased Osmotic Fragility

Splenomegaly

Gall stones

Question: Which of the following is not seen in Hereditary Spherocytosis Choices: A. Direct Coomb's Positive B. Increased Osmotic Fragility C. Splenomegaly D. Gall stones Answer:

Cleft lip, polydactyly, Holoprosencephaly are characteristic feature of?

Down syndrome

Edward syndrome

Patau syndrome

Turners syndrome

Question: Cleft lip, polydactyly, Holoprosencephaly are characteristic feature of? Choices: A. Down syndrome B. Edward syndrome C. Patau syndrome D. Turners syndrome Answer:

NOT a feature of Holt Oram Syndrome is

Absent Radius

Atrial septal defect

Thrombocytopenia

Autosomal dominant inheritance

Question: NOT a feature of Holt Oram Syndrome is Choices: A. Absent Radius B. Atrial septal defect C. Thrombocytopenia D. Autosomal dominant inheritance Answer:

Treatable causes of dementia are -a) Alzheimer's ds.b) Hypothyroidismc) Multi-infarct dementia d) SDH (subdural h'ge) e) Hydrocephalus

abc

ade

bde

bce

Question: Treatable causes of dementia are -a) Alzheimer's ds.b) Hypothyroidismc) Multi-infarct dementia d) SDH (subdural h'ge) e) Hydrocephalus Choices: A. abc B. ade C. bde D. bce Answer:

Reversible cause of dementia -a) Post encephalitisb) Multi infarctc) Hydrocephalusd) Senile dementia

a

bc

ad

ac

Question: Reversible cause of dementia -a) Post encephalitisb) Multi infarctc) Hydrocephalusd) Senile dementia Choices: A. a B. bc C. ad D. ac Answer:

Causes of breech presentation are:a) Hydrocephalusb) Oligohydramniosc) Pelvic contracture d) Placenta praevia

acd

ad

bc

bde

Question: Causes of breech presentation are:a) Hydrocephalusb) Oligohydramniosc) Pelvic contracture d) Placenta praevia Choices: A. acd B. ad C. bc D. bde Answer:

Hydrocephalus in the fetus is diagnosed by all except :

Large fontanelle with widely separated sutures as felt on PV examination

High floating head

Serial ultrasound

CPD

Question: Hydrocephalus in the fetus is diagnosed by all except : Choices: A. Large fontanelle with widely separated sutures as felt on PV examination B. High floating head C. Serial ultrasound D. CPD Answer:

In Hydrocephalus ex vacuo, the compensatory enlargement of ventricles and an increase in CSF volume due to brain atrophy is seen in-

Alzheimers diseae

Picks diseases

Both

None of the above

Question: In Hydrocephalus ex vacuo, the compensatory enlargement of ventricles and an increase in CSF volume due to brain atrophy is seen in- Choices: A. Alzheimers diseae B. Picks diseases C. Both D. None of the above Answer:

Normal pressure Hydrocephalus is characterized by all except -

Aphasia

Dementia

Ataxia

Urinary incontinence

Question: Normal pressure Hydrocephalus is characterized by all except - Choices: A. Aphasia B. Dementia C. Ataxia D. Urinary incontinence Answer:

In Hydrocephalus exvacuo, the compensatory enlargement of ventricles and increase in CSF volume due to brain atrophy is seen in-

Alzheimers diseae

Picks diseases

Both

None of the above

Question: In Hydrocephalus exvacuo, the compensatory enlargement of ventricles and increase in CSF volume due to brain atrophy is seen in- Choices: A. Alzheimers diseae B. Picks diseases C. Both D. None of the above Answer:

Hydrocephalus is detailed best antenatally by –

X-ray abdomen

Amniocentesis

Clinical examination

Ultrasonography

Question: Hydrocephalus is detailed best antenatally by – Choices: A. X-ray abdomen B. Amniocentesis C. Clinical examination D. Ultrasonography Answer:

Disease having autosomal recessive inheritance -a) Cystic fibrosisb) Hydrocephalusc) Duchene muscular dystrophyd) Albinisme) Vitamin D resistant ricket

b

ad

ac

ab

Question: Disease having autosomal recessive inheritance -a) Cystic fibrosisb) Hydrocephalusc) Duchene muscular dystrophyd) Albinisme) Vitamin D resistant ricket Choices: A. b B. ad C. ac D. ab Answer:

Hair on end appearance is seen in X–ray skull in –a) Thalassemiab) Hydrocephalusc) Chronic malariad) Sickle cell anemia

ad

c

ac

ab

Question: Hair on end appearance is seen in X–ray skull in –a) Thalassemiab) Hydrocephalusc) Chronic malariad) Sickle cell anemia Choices: A. ad B. c C. ac D. ab Answer:

Which of the following is true about TB meningitis-a) Exudates are formed on the convexities of brainb) CSF stored at 4°C in the time of transportationc) Hydrocephalus is common sequalaed) Meningoencephalitis is common manifestation

abc

bcd

ac

bd

Question: Which of the following is true about TB meningitis-a) Exudates are formed on the convexities of brainb) CSF stored at 4°C in the time of transportationc) Hydrocephalus is common sequalaed) Meningoencephalitis is common manifestation Choices: A. abc B. bcd C. ac D. bd Answer: