NEUROLOGY MCQ – Exercise 34

The multiple choice questions in this online test paper focuses on NEUROLOGY MCQ. If you are looking for self evaluation of your PG Medical entrance exam preparation then this online NEUROLOGY MCQ Test Paper will help you to evaluate your exam preparation.

Instruction for REPRODUCTIVE BIOLOGY/ REPRODUCTIVE MEDICINE / INFERTILITY MCQs:

1- This online MCQ practice test paper contains 30 questions.
2- Each question in this online practice test paper have four options and only 1 option is correct.
3- You can view the answers of this practice test paper after submitting the practice test paper.
Note: The answers mentioned at the end of practice test are the best suitable option as per our knowledge. Users shall cross-check the answers with their textbooks.

Q 1. which SMA (spinal muscular atrophy) carries worst prognosis

SMA I

SMAII

SMA III

none of the above

Q 2. differential diagnosis of ALS is

compression of cervical spinal cord

thyrotoxicosis

chronic lead poisoning

all of the above

Q 3. intranuclear inclusions `Bunia bodies` are a pathognomic feature of

motor neuron disease

multiple sclerosis

subacute combined degeneration of cord

myasthenia gravis

Q 4. telangiectasia in AT usually occurs on

nil bed

intracranial

bulbar conjunctiva

all of the above

Q 5. in ALS the leading cause of death includes

infections

depression and suicide

respiratory paralysis

cardiovascular event

Q 6. laboratory tests useful in the diagnosis of AT is

cryofibrinogen

ceruloplasmin level in blood

AFP level in blood

apolipoprotein A-1

Q 7. only upper motor neurons innervating the brainstem and spinal cord are effected in

pseudobulbar palsy

PLS

FSP

all of the above

Q 8. chronic sporadic motor neuron disease with predominant involvement of lower motor neurons is

multifocal motor neuropathy with conduction block

motor predominant peripheral neuropathy

motor neuropathy with paraproteinemia

all of the above

Q 9. Kugelberg-Welander disease is SMA (spinal muscular atrophy)

SMA I

SMAII

SMA III

none of the above

Q 10. which of the following is false for familial spastic paraplegia in adults

X linked transmission

presents in3rd or 4th decade

progressive spastic weakness inlower extremities

long survival

Q 11. in ALS the structure that is left intact includes include

motor neurons for ocular motility

parasympathetic neurons in sacral spinal cord

sensory apparatus

all of the above

Q 12. in AT most consistent defect of the lymphoid system includes

poorly developed or absent thymus gland

generalized lymphadenopathy

splenomegaly

lymphedema

Q 13. true regarding spinal muscular atrophy

extensive loss of large motor neurons

evidence of denervation atrophy on muscle biopsy

electrophysiologic evidence of denervation

all of the above

Q 14. neuroprotective properties exhibited by which antibiotics

azithromycin

minocycline

spiramycin

vancomycin

Q 15. Werdnig-Hoffmann disease is SMA (spinal muscular atrophy)

SMA I

SMAII

SMA III

none of the above

Q 16. acute sporadic motor neuron disease includes

poliomyelitis

herpes zoster

coxsackie virus

all of the above

Q 17. true regarding Kennedy`s disease include

X linked spinobulbar muscular atrophy

lower motor neuron disorder

gynecomastia and reduced fertility

all of the above

Q 18. in ALS the structure that is left intact includes

sensory apparatus

center for control and coordination of movement

center for cognitive process

all of the above

Q 19. true regarding AT

present in first decade of life

progressive telangiectatic lesions with deficits in cerebellar function and nystagmus

high incidence of recurrent pulmonary infections and neoplasms of lymphatic and reticuloendothelial system

all of the above

Q 20. true regarding Fazio-Londe syndrome

ALS variant

juvenile onset

involves musculature innervated by brainstem mainly

all of the above

Q 21. MMCB (multifocal motor neuropathy with conduction block) evolves in association with

tuberculosis

multiple myeloma

syphilis

all of the above

Q 22. true regarding familial spastic paraplegia includes

sexually function preserved

spastin and atlastin gene mutations common

degeneration of corticospinal tracts

all of the above

Q 23. true regarding MMCB

elevated serum titers of mono and polyclonal antibodies to ganglioside GM1

no corticospd to IVIGinal tract signs

respond to IVIG

all of the above

Q 24. feature of ALS include all except

raised proteins in CSF

absence of pain or of sensory changes

normal bowel and bladder function

normal roentgenographic studies of spine

Q 25. Lou Gehrig`s disease is other anme of

ALS

myasthenia gravis

multiple sclerosis

subacute combined degeneration of cord

Q 26. chronic sporadic motor neuron disease with predominant involvement of upper motor neurons is

ALS

Primary lateral sclerosis

motor neuropathy with paraproteinemia

multifocal motor neuropathy with conduction block

Q 27. true regarding spinal muscular atrophy

genetic lower motor neuron disease

early onset

locus on chromosome 5

all of the above

Q 28. hereditary forms of mitochondrial cytopathies include

Kearns –Sayre syndrome

MERRF

MELAS

all of the above

Q 29. true regarding AT

affected child has normal intelligence

hypersensitivity to ionizing radiation

predisposition to malignancy present

all of the above

Q 30. Riluzole-a glutamate antagonist is useful in the treatment of

ALS

multiple sclerosis

subacute combined degeneration of spinal cord

myasthenia gravis

NEUROLOGY MCQ – Exercise 34

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NEUROLOGY MCQ – Exercise 34

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