Page 1 of 2: 2008 bhu paper

nitty · Credits: 879 My Scrapbook

1...zelwegwers syd means absenc e of
mitochon
lysososme
perox

2..martinotti cells in
medula
cerebelun

3.colpocephaly
agenesis of corpus calosum
hydroceph

4..open spinal dysgraphism in
meninigioma
epidermoid

5..scimtars sign in
tapvc
ms

6.
laugier femoral hernia
hydrocele in sac
...
....
..

7 dawson criteria of lymfoma does not incll
..peri neuropathy
adjavent organ

8..shunt wich prevents rebleed is
side 2 side portocaval
end 2 end

9...increasd neonatal morbidty in
latent arrest
secondary arest

10.some q on pathological fracture

11..serovar listeria mc
1a
2b

12..behavioural system does nt incl
organisation design
personal management
network analysis

13..world popln wil bcom 8 milion in wich year

14..vestibular neuronitis tt is
cinnazarine
...

15 osteoarthritis earliest change
dec space on middle condyle
inc space on lat condyle

16..post hip dislocn mc after replacement in
oa
ra

17,,submand gland excision n not involved is
lingual
hypoglossal

18 g.i gangrene mc in
mercurichrome pois
...

19.retrobul inj does nt in
3 cn
4th cn
6 cn
ciliary n nd ganglion

20..polydixone is all ex
single suture filament
hyrolyses

21 paraduod fossa
open inf blind sup
open sup blind inf
open ant bilnd post

22..perineal memb pierced by all ex..
clitoris
bulbourethral gland

23..lining of ductus defrens
simple columnar
starified columna
sq stratified columna

24..moderately hard water
3-6
6-10

25..clergyman knee is

saarthi · Credits: 1249 My Scrapbook

1.Polydixanone(PDS) sutures true a/e:
1.its a monofilament
2.a polyamide dimmer
3.50% tensile strength left after 4 wks
4. Absorbed by hydrolysis

2 Intra alveolar pressure:
1. -1 of atm pressure.
2.+1 of atm pressure
3. -10 of atm pressure
4. +10 of atm pressure

3.Non obstructive cause of tracheostomey:
1. Ludwigs angina
2. ca larynx
3.B/L add palsy
4. B/L Abd palsy

4.Death in penile ca, cause:
1.cachexia
2. Sec. hemorrhage

5.Splenectomy c/c:
1. Gastric dialation
2. Pancreatic fistula
3. Dudenal fistula
4. Hemorrhage

6. Kawasaki ds not found:
1. Truncal rach
2. thrombocytopenia
3. pericarditis
4. Post cervical lymedenopathy

7. Eosinophilia , necrotic small medium sized vs:
1. P.A.N
2. Chrug str.
3. Wegeners
4.Kawasaki

8. moderate Hardness:
1. 0-1
2. 1-3
3. 3-6
4. >6

9. Prostate adenoma > 80gms, >3cm multiple stones in prostate. TOC:
1. Filler operation
2. M…… operation
3. TURP
4. LASER operation

10. Long standing solitary nodule in lung due to:
Thyroid ca
Collageneous ca
GIT ca
…..

11. Vestibular neuritis TOC:
Epley manuover

12.Rotator cuff cavity b/w:
Supraspinatus & infraspinatus
Supraspinatus & teres major
Supraspinatus & subscapularis
…..

13. Perineal membrane not pierced by :
1. Deep br of ….
2.Dorsal ar of penis
3. Perineal br of femoral nr.
4. Bulbourethral gland

14. Retro bulbar Anaesthesia not involved
5th cr nr
4th cr nr
6th cr nr
……

15. osteoarthritis 1st sign
Loose bodies ..
Dec lateral space

16. Most reliable sign of carpel tunnel syn:
Pain
Pallor
Poor radial pulse

17. Scaphoid fracture m/m:
Crape bandage & x ray after 2 wks
POP cast & review X ray after 2 wks

18. Section 142 IPC:
Cross questioning
Any question can be asked
Telephonic recording
Objective evedience

19. After hip replacement, post dislocation is due to:
Ankylosing spondylosis
RA
Osteoarthritis

20 capsule + slime present is:
Bacillus anthrax
Kleibsella
Streptococcus pneum
Streptococcus salivarus

21 Leptospirosis most dangerous strain:
1\2a
1\2b
4b
4d

22. Glander`s ds
Brucella mallei
Brucella pseudo mallei

23 Recurrent diarrhea in HIV t/t:
Octreotide
Sulfasalasine
Codeine
Dilax..

24 If each value is multiplied by 10 ,change in SD
*10
-10
/10
No change

25 Action of stapideus:
A. Stapes pulled inward , mallus inward,incus superiorly
B.
C.
D.

26 Paraduodenal abscess:
1.open superiorly, inferiorly blind sac
2.vice versa of this
3. open right & blind sac to left
4.vice vers a of this

27. Not used in eye:
Propofol
Xylocaine
Bupivacaine
Cinchocaine

28 GFR inc , what happens
-no change
-prox absorbtion inc
- prox absorbtion inc by 78 %
-both prox & dist absortion inc

29 After birth ,neonate present with cyanosis. Relieved when given PGE2
&ballon septoplasty done . Diagnosis:
TOF
Truncus arteriosus
Tricuspid atresia
TGA

30 Marquis test for:
Opium
Organophosphate
Organochlorine
….

31 Thrombocytopenia + eczema:
Wiscott Aldrich syn

32.Why preg is diabetogenic a/e:
-glucose secreted more
-insulin resistance
-Foetus uses alanine & other gluconeogenic AA
-dec lipolysis

33 Most splenic shunt:
End to end
Side to side
War…..
….

34 Auto immune, oligoclonal band..
-Multiple sclerosis
-Creuz Jacob ds

35 Stored RBC
-loose Na
-K inc inside
-
-lesser destruction in hypovolumic sol

36. Diff b/w embolic stroke & thrombotic stroke a/e:
-seizure
-heatrt ds
-Rapid onset
-

rohkav12 · Credits: 2777 My Scrapbook

Zellweger Syndrome

Zellweger syndrome is a rare, congenital (present at birth) disorder characterized by the reduction or absence of peroxisomes (cell structures that rid the body of toxic substances) in the cells of the liver, kidneys, and brain.

Zellweger syndrome is one of a group of genetic disorders called the leukodystrophies that affect growth of the myelin sheath, the fatty covering--which acts as an insulator--on nerve fibers in the brain. The most common features of Zellweger syndrome include an enlarged liver, high levels of iron and copper in the blood, and vision disturbances. Some affected infants may show prenatal growth failure. Symptoms at birth may include lack of muscle tone and an inability to move. Other symptoms may include unusual facial characteristics, mental retardation, seizures, and an inability to ^*&^* and/or swallow. Jaundice and gastrointestinal bleeding may also occur.

There is no cure for Zellweger syndrome, nor is there a standard course of treatment. Infections should be guarded against to prevent such complications as pneumonia and respiratory distress. Other treatment is symptomatic and supportive.

The prognosis for individuals with Zellweger syndrome is poor. Death usually occurs within 6 months after onset, and may be caused by respiratory distress, gastrointestinal bleeding, or liver failure.

Information provided by the
National Institute of Neurological Disorders and Stroke
National Institutes of Health

rohkav12 · Credits: 2777 My Scrapbook

Martinotti cells are small multipolar neurons with short branching dendrites. They are scattered throughout various layers of the cerebral cortex, sending their axons up to the cortical layer I where they form axonal arborization. The arbors transgress multiple columns in layer I and make contacts with the distal tuft dendrites of pyramidal cells. [1]

Recent research suggests that Martinotti cells are associated with a cortical dampening mechanism. When the pyramidal neuron, which is the most common type of neuron in the brain, starts getting over excited, Martinotti cells start sending inhibitory signals to the surrounding neurons. [2]

Martinotti cells were fist described in 1888 by Giovanni Martinotti, an Italian physician

rohkav12 · Credits: 2777 My Scrapbook

Colpocephaly: A brain disorder in which there is an abnormal enlargement of the occipital horns of the brain --the posterior or rear portion of the lateral ventricles (cavities or chambers) of the brain. This enlargement occurs when there is an underdevelopment or lack of thickening of the white matter in the posterior cerebrum.

Colpocephaly is characterized by microcephaly (abnormally small head) and mental retardation. Other features may include motor abnormalities, muscle spasms, and seizures.

The cause of colpocephaly is unknown. A disturbance occurs between the second and sixth months of pregnancy.

Colpocephaly may be diagnosed late in pregnancy, although it is often misdiagnosed as hydrocephalus (excessive accumulation of cerebrospinal fluid in the brain). It may be more accurately diagnosed after birth when signs of mental retardation, microcephaly, and seizures are present.

There is no definitive treatment for colpocephaly. Anticonvulsant medications can be given to prevent seizures, and doctors try to prevent contractures (shrinkage or shortening of muscles). The prognosis for individuals with colpocephaly depends on the severity of the associated conditions and the degree of abnormal brain development. Some children benefit from special education.

nitty · Credits: 879 My Scrapbook

thanx rohnav plz add to more ans

1..ct in epilepsy don e in al except
siezures after 20ys of age
easy to comtrol siezure

2..verucous ca
doest not metastsise
treted by cruyotherapy
recurs after local tt

3..misoprostol
m serious s/e is diarrhoea
used for contraception wid mifepristone

4..all r retention cyst except
pcod
dysgerminoma

5...edingr westfal nucleus is
general somatic efferent

6..6 dioptres defect not done 4 tt is
lasik
lasek
prk
aphakic lens replacement

7...enxymes of gluconeogenesis r alll ex cept
py caboxylase
pep caboxykinase
hexokinase

8..operation reqd in non obstructiv lesion of larynx in
ca larynx
add palsy
abd palsy
ludwings angina

9...plaques in brain wid abn bands in csf in
muliple sclerosis
alzhiemers

10....macrophage like cels wid pneumonia n buding in
paracocci
coccido
blastomycosis
histoplamosis

11...pr of lung during expiration is
-1mmhg
-10

how much cut off u guys expect i n this paper ..
when is result goin to get out????

nadu · Credits: 17258 My Scrapbook

good going guys!

nitty · Credits: 879 My Scrapbook

cong adrenal hyperplasia is not seen in
1..17alfa defi
2 17 beta defi
3..21 alfa defi
4..11alfa defi

nitty · Credits: 879 My Scrapbook

cong adrenal hyperplasia is not seen in
1..17alfa defi
2 17 beta defi
3..21 alfa defi
4..11alfa defi

DOCTORSHRADDHA · Credits: 3023 My Scrapbook

hello can u tll me how u prepared for BHU i mean is there any old question bank n wat topics

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