renal pediatric
TRANSCRIPT
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Renal MCQs
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A 6-year-old boy presents with tea-colored urine. Hewas diagnosed with an upper respiratory tract infection2 days ago. His parents report that a siilar episodeoccurred ! onths ago. "here is no history of traua.#indings include$ blood pressure% &'()*' Hg+teperature% ,C /&''.!#0+ and absence of rash or
1oint abnoralities. eru copleent le3el is noral.
"he M4" li5ely eplanation of these findings is
A. Alport hereditary nephritis
7. idiopathic hypercalciuria
C. iunoglobulin A nephropathy /7erger disease08. postinfectious acute gloerulonephritis
&. 9. thin gloerular baseent ebrane nephropathy
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A 2-wee5-old ale infant is being seen for a routine healthsuper3ision 3isit. :hysical eaination re3eals adistended abdoen% and the bladder can be palpatedabo3e the syphysis pubis. "he other has noticed thaturine ;dribbles< fro his urethra.
4f the following% the M4" li5ely diagnosis is
A. posterior urethral 3al3es
7. prune belly syndroe
C.urethral di3erticula8.urethral eatal stenosis
9. urethral stricture
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Question . 6. A (-yr-old girl presents with cola-colored urine% oliguria%and
body edea 2 w5 after being treated for group A -heolyticstreptococcal
pharyngitis. Her copleent C, is noted to be 3ery low at &( g)d=.
>henshould this patient?s copleent C, le3el be repeated in order to
confir
your suspected diagnosis@
A0n & wee5
70n 2 w5
C0n , w5
80n ! w5
90n w5
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Question . ,. "he presence of renalparenchyal scarring due to
3esicoureteral reflu is best deterined by$
A0 8MA scan
70 Renal ultrasonography
C0 BCD
80 C" scan
90 ntra3enous pyelography
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Q0 All true about Ditlan syndroe ecept $
A0 Metabolic al5alosis.70 Hypo5aleia.
C0 Hypertension.
80 Hypocalcuria.
90 Hypoagneseia
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Question . !(. An asyptoatic &6-yr-old African-Aericangirl with
hypertension is found to ha3e ,E proteinuria by dipstic5testing on id-day
and first orning 3oided urine saples. "he icroscopicanalysis shows '-2 red blood cells per high-power field."he ost li5ely diagnosis is$
A0:ostinfectious gloerulonephritis
708iabetic nephropathyC0 Minial-change disease
80 #ocal segental gloerulosclerosis
90 =upus nephritis
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Question . !F. A ,-yr-old girl presents to the eergencydepartent with
anasarca. "he urinalysis shows !E proteinuria and isnegati3e for blood.
eru albuin is &.2 g)d= and seru creatinine is '.!g)d=. "he ost
li5ely diagnosis is$
A0 :ostinfectious gloerulonephritis
70 Minial-change disease
C0 gA nephropathy
80 =upus nephritis
90 #ocal segental gloerulosclerosis
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Question . (!. A &'-yr-old girl presents with edea and grossheaturia. Her
e3aluation re3eals seru creatinine &.! g)d=% seru albuin 2.,g)d=% 2!-
hr urine protein ecretion (.( g% and C, &2 g)d=. "he ost li5ely
cause of hernephrotic syndroe is$
A0 Mebranoproliferati3e gloerulonephritis
70 Minial-change disease
C0 gA nephropathy80 Mebranous nephropathy
90 #ocal segental gloerulosclerosis
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Question . &6. An -yr-old girl presents with dysuria% abdoinal pain%and
interittent pin5 urine. A urinalysis re3eals specific gra3ity of &.'2'% pHof 6.'%
2E heaturia% no protein% and (' red blood cells per high-power field. A
2!-hrurine specien re3eals 6 g)5g body weight of calciu. >hich of the
following is an acceptable treatent for this patient?s proble@
A0ncreased inta5e of sodiu-containing fluids
708ietary calciu restrictionC0ingle daily dose of hydrochlorothiaGide
80Bitain 8 suppleentation
90Bitain C suppleentation
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Question . 2,. All of the following stateents regardingpoststreptococcal
gloerulonephritis /:D0 are true ecept$
A0 :D is coon in children 2 to ( yr of age
70 "he acute phase of :D usually resol3es in 6- w5C 0 Microscopic heaturia ay persist for &-2 yr following the
initial presentation of :D
80 "he seru C, le3el is usually reduced in the acute phase
of :D
90 "he best single antibody titer to docuent cutaneousstreptococcal infection is the deoyribonuclease /8ase0
7 antigen
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Iou are e3aluating an -year-old girl in your office who hasfe3er and ild abdoinal pain. :hysical eainationre3eals a teperature of !'.'C /&'!.'#0 and a soft andnontender abdoen without flan5 or suprapubictenderness. rinalysis and icroscopy are negati3eecept for a positi3e dipstic5 test of &'' g)d= of protein/E20.
4f the following% the M4" li5ely cause of the proteinuria is
A. collagen 3ascular disease
7. high fe3erC.nephrotic syndroe
8.postinfectious acute gloerulonephritis
9. urinary tract infection
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Question . ((. A newborn infant de3elops anasarca andpoor urine output
during the first wee5 of life. eru creatinine is '., g)d=and seru albuin
is &.' g)d=. >hich of the following clinical findings is leastli5ely@
A0 9nlarged placenta
70 :reaturity
C0 Rapid response to steroid therapy
80 9le3ated aternal seru -fetoprotein
90 Massi3e proteinuria
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Question . 6!. A &!-yr-old girl de3elops acute renal failurerelated to Henoch-
ch nlein purpura gloerulonephritis. =aboratory findingsay include all of
the following ecept$
A0 Hypercalceia
70 Hyper5aleia
C0 Hyponatreia
80 Hyperphosphateia
90 Hypoalbuineia
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Question . 2. Ris5 factors for urinary tractinfections include all of the
following ecept$
A0ncircucised penis
70 eual acti3ity
C0 Reflu nephropathy
80 8ouble-ureter systes
90 Chronic use of antibiotics
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A &(-year-old boy presents with red urine following footballpractice. #indings on physical eaination are noral.rinalysis re3eals pH% 6.'+ specific gra3ity% &.'2'+ blood%E!+ protein% trace+ and ' to 2 red blood cells per high
power field.Aong the following% the M4" li5ely eplanation for the
red color of the urine is
A. heaturia
7. ingestion of food coloringC.yoglobinuria
8.presence of urates
9. traua
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n addition to 3ascular throbosis% the M4"li5ely coplications obser3ed in childrenwho ha3e inial-change nephrotic
syndroe are$A. acute renal failure
7. chronic renal failure
C. hypercholesteroleia8. hypernatreia
9. hyponatreia
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Question . &,. A ,-yr-old girl presents to your office with acute onset of
lethargy and pallor. "he child?s other reports that the child had bloody
diarrhea for ( days that cleared one day prior to presenting to youroffice. he
also notes acute onset of cola-colored urine. 4n eaination% the
patient ispale and lethargic. 7lood pressure is &2')' Hg. "he ost
appropriate
net step in diagnosis would be$
A0rinalysis
70J-ray eaination of the abdoen
C0rine culture
80Coplete blood cell count
90:rothrobin tie
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A 2-onth-old infant is e3aluated for 3oiting and diarrhea.#indings include$ edea+ abdoinal distension+ widefontanelles and cranial sutures+ blood pressure% &'')6' Hg+ urinalysis% E! protein+ and seru albuin% &.2g)d=. "he other says that she had preeclapsia andthat the placenta was large. Iou suspect congenitalnephrotic syndroe.
"he M4" iportant anageent strategy for a goodoutcoe is
A. adinistration of 2(K albuin and furoseide
7. adinistration of high-dose corticosteroids
C. intensi3e edical follow-up% including referral for dialysisand renal transplantation
8. restriction of dietary protein
9. restriction of fluid and salt inta5e
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Iou are eaining a &-day-old girl who was deli3ered3aginally at ter. :renatal fetal ultrasonography had
re3ealed the presence of left hydronephrosis. 4nphysical eaination% blood pressure is *()(' Hg%and the abdoen is soft% with palpable fullness in theright flan5.
4f the following% the M4" li5ely diagnosis is
A. posterior urethral 3al3es
7. ureterocele
C.ureteropel3ic 1unction obstruction8.uretero3esical obstruction
9. 3esicoureteral reflu
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Question . !,. rine dipstic5 testing of a specien obtainedfro a febrile !-
yr-old child with acute 3iral gastroenteritis shows specificgra3ity &.','% pH
(.'% 2E proteinuria% and no blood cells. "he ost li5elycause of the patient?s
proteinuria is$
A0 "ransient proteinuria
70 ephrotic syndroe
C0 4rthostatic proteinuria80 Acute gloerulonephritis
90 Chronic gloerulonephritis
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Question . 2. A ,-yr-old boy presents to your office with sudden onset of cola
colored urine% progressi3e facial swelling o3er the past , days% and decrease
urine 3olue o3er the past day. His eaination is notable for blood pressur&,')' Hg% periorbital edea% bibasilar rales% and an5le swelling. His
urinalysis is rear5able for ,E heaturia% &E proteinuria% &'' red blood cells
per high-power field% and red blood cell casts. His seru electrolytes are
noral and the seru albuin is ,.2 g)liter. "his clinical presentation is os
consistent with$
A0Acute renal failure
70Acute pyelonephritis
C0ephrotic syndroe
80Acute gloerulonephritis
90Chronic renal failure
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Question . (. A &(-yr-old boy with a &2-yr history of icroscopicheaturia is
noted to ha3e bilateral high-freLuency sensorineural hearing loss%blood
pressure of &!')F' Hg% seru creatinine of &.( g)d=% and urinary
proteinof 2%''' g)2! hr. "his patient?s other also has icroscopic
heaturia. "he
ost li5ely ode of inheritance for this child?s gloerular disease is$
A0Autosoal doinant with incoplete penetrance
70J-lin5ed doinant
C0Autosoal recessi3e
80J-lin5ed recessi3e
90Autosoal doinant
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Iou disco3er a right-sided% palpable abdoinal ass in anewborn ale who has had an uncoplicated perinatalcourse. =aboratory e3aluation re3eals$ creatinine% '.*g)d=+ noral findings on urinalysis+ and platelet count%
,('%''').4f the following% the M4" li5ely cause of this ass is
A. autosoal recessi3e polycystic 5idney disease
7. idgut 3ol3ulus
C. renal 3ein throbosis8.ureteropel3ic 1unction obstruction
9. >ils tuor
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A (-year-old girl 3isited her doctor 2 wee5s ago to treat a sore throat.He prescribed an antibiotic that she too5% but the parents cannotrecall its nae. he presents at the eergency departent todaywith gross heaturia and periorbital edea. he has a blood
pressure of &(')F( Hg. "he attending physician suspects shehas acute postinfectious gloerulonephritis /:AD0. rinalysisre3eals too nuerous-to-count red blood cells and 2E protein. "oconfir the diagnosis% you easure seru copleent le3els+ theC, is (* g)d= /(.* g)=0 /low0 and the C! is 2! g)d= /2.! g)=0/noral0. >ithin , days% the gross heaturia and hypertensionresol3e spontaneously. i wee5s later you see her in your office.
4f the following% the laboratory results that would be consistent withresol3ing :AD are$
C, Heaturia :rotein
A. =ow Microscopic egati3e
7. =ow Microscopic :ositi3e
C. oral Microscopic egati3e8. oral Microscopic :ositi3e
9. =ow one egati3e
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Iou are eaining a newborn in the nursery and
palpate a large ass in the abdoen.
4f the following% the M4" li5ely diagnosis is$
A.autosoal doinant polycystic 5idney disease
7.horseshoe 5idney
C. ulticystic 5idney dysplasia8. renal 3ein throbosis
9.>ils tuor
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A (-year-old boy who has nephrotic syndroe hasde3eloped anasarca. #indings include$ blood pressure%F')6' Hg+ blood urea nitrogen% !' g)d=+ creatinine%
'.6 g)d=+ albuin% &.( g)d=+ noral C, le3el+ and !Eproteinuria. After recei3ing furoseide% he lost 2 = of fluidbut de3eloped abdoinal pain% heaturia% andhypertension. rinalysis shows N&'' red blood cells perhigh-power field.
4f the following% the M4" li5ely diagnosis is
A. acute gloerulonephritis
7. acute tubular necrosis
C.heorrhagic cystitis
8. interstitial nephritis
9. renal 3ein throbosis
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Question . 2. A !-o-old boy is noted to ha3e poor growthat a routine well
child 3isit. Results of laboratory studies include serusodiu &!' ol)=%
potassiu ,.( ol)=% chloride &&6 ol)=% andbicarbonate &, ol)=. All of
the following should be considered in the differentialdiagnosis ecept$
A0 8istal renal tubular acidosis
70 Chronic diarrhea
C0 :roial renal tubular acidosis
80 =actic acidosis
90 Renal #anconi syndroe
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A (-year-old boy presents with flan5 pain and short stature.#indings include$ creatinine% '.( g)d=+ sodiu% &,F9L)=+ potassiu% ,. 9L)=+ chloride% &&, 9L)=+bicarbonate% &( 9L)=+ calciu% F.' g)d=+ phosphorus%!.' g)d=+ urinalysis% ( to 2' red blood cells per high-power field+ plain radiography% bilateral renalcalcifications.
"he M4" li5ely cause of these renal calcifications is
A. cystinuria
7. distal renal tubular acidosis /type &0C.priary hyperparathyroidis
8.proial renal tubular acidosis /type 20
9. 3itain 8 intoication
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Iou are e3aluating a 2-onth-old infant for icroscopicheaturia. He has a history of respiratory distresssyndroe and bronchopulonary dysplasia andcurrently is recei3ing caffeine and furoseide. rinalysisre3eals$ specific gra3ity% &.'&'+ pH% 6.(+ &( to 2' red
blood cells+ no protein+ and ' to 2 white blood cells.9lectrolyte le3els are noral.
4f the following% the M4" li5ely cause of the heaturia is$
A. benign failial heaturia
7. hypercalciuriaC.ulticystic 5idney dysplasia
8.tuor
9. urinary tract infection
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he other and aternal grandfather of a 6-onth-old boyboth ha3e Alport syndroe.
4f the following% the M4" appropriate stateent toinclude in counseling this boy?s other about Alport
syndroe is that$A. affected boys freLuently suffer fro acroparesthesias
7. the boy has an increased ris5 for de3eloping >ils tuor
C. the disorder is ore se3ere in ales than in feales
8. there is a 2(K chance that her son has Alport syndroe9. there is no need to onitor her son for coplications of
the disorder until he is
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rinalysis obtained during a health super3ision 3isit of a &'-year-old boy re3eals 2E protein. "he reainder of theurinalysis is noral. Results of faily and personaledical histories as well as physical eaination of theboy are negati3e.
4f the following% the 79" net step is to$
A. arrange consultation with a nephrologist
7. eaine the urine of faily ebers
C.obtain a 2!-hour urine saple for protein Luantification8.obtain renal ultrasonography
9. perfor a urinalysis on the first orning 3oid
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4ne onth ago% a &'-year-old boy presented to you with edea of theface% hands% and feet. rinalysis re3ealed 2' to 2( red blood cellsand !E protein. Iou diagnosed nephrotic syndroe and placed hion a recoended regien of oral steroids. His face now ehibitscushingoid features% but his edea has not subsided. rinalysistoday re3eals !E protein and oderate blood.
4f the following% the M4" li5ely diagnosis at this tie is$
A. focal segental gloerulosclerosis
7. Henoch-chOnlein purpura
C. iunoglobulin A nephropathy
8. inial-change nephrotic syndroe9. postinfectious acute gloerulonephritis
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A newborn ale has ecess abdoinal s5in%deficiency of the abdoinal usculature% andcryptorchidis.
4f the following% the M4" li5ely etiology of thesefindings is$
A.chronic aniotic fluid lea5age during pregnancy
7.early urethral obstruction
C.etrophy of the bladder8.polycystic 5idneys
9.renal agenesis
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A prenatal ultrasonographic eaination of a alefetus at ,2 wee5s? gestation re3eals bilateralrenal aplasia.
>hen the infant is deli3ered se3eral wee5s later%
the condition M4" li5ely to be e3ident is$
A.bladder wall hypertrophy
7.cryptorchidis
C. incoplete de3elopent of the sacru
8. prune belly /wrin5led abdoinal s5in0
9.pulonary hypoplasia
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A &,-onth-old child has growth retardation% polyuria andpolydipsia. Results of laboratory e3aluation include$seru creatinine% &*.* col)= /'.2 g)d=0+ blood ureanitrogen% ,.(* ol)= of urea /&' g)d=0+ sodiu% &,(
ol)= /&,( 9L)=0+ potassiu% , ol)= /, 9L)=0+chloride &&2 ol)= /&&2 9L)=0+ bicarbonate% &, ol)=/&, 9L)=0+ calciu% 2.&* ol)= /.* g)d=0+phosphorus% 2.' g)d=+ uric acid% 2.' g)d=+ seruglucose% (.' ol)= /F' g)d=0+ generaliGed ainoaciduria+ phosphaturia+ 5aliuresis+ and glycosuria.
4f the following% the M4" appropriate test to define theetiology of this child?s illness is
A. antidiuretic horone le3els
7. leu5ocyte cystine le3elsC.plasa renin acti3ity
8.seru agnesiu
9. slitlap eaination
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A 2-year-old girl is aditted to the hospital for treatent ofdehydration and diarrhea. nitial laboratory e3aluationshowed$ seru creatinine% *'.* col)= /'. g)d=0+blood urea nitrogen% &!., ol)= of urea /!' g)d=0+
sodiu% &,( ol)= /&,( 9L)=0+ potassiu% ! ol)=/! 9L)=0+ chloride% &'' ol)= /&'' 9L)=0+bicarbonate% &( ol)= /&( 9L)=0+ urine pH% (.'+ urinesodiu% &' ol)= /&' 9L)=0+ urine potassiu% &'ol)= /&' 9L)=0+ and urine chloride% !' ol)= /!'9L)=0. 8espite hydration% a noral anion gap etabolicacidosis persists.
4f the following% the M4" li5ely diagnosis is
A. acute renal failure
7. chloride-losing nephropathyC.etrarenal losses of bicarbonate
8. renal tubular acidosis% type B
9. renal tubular acidosis% type
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A ,-year-old girl presents with fe3er% left flan5 pain% anddysuria. 4n physical eaination% blood pressure is &'')(
Hg% teperature is ,FC /&'2.2#0% and there is leftcosto3ertebral angle tenderness. A catheriGed urine culturegrows ore than &''%''' C#), of 9scherichia coli.Results of renal ultrasonography are noral% and 3oidingcystourethrography shows bilateral grade , 3esicoureteralreflu /BR0. Iou prescribe antibiotics for &' days.
4f the following% the net 79" step is
A. no prophylais
7. periodic urine cultures for 6 onths
C.prophylais with antibiotics for 6 onths8.prophylais with antibiotics until the BR resol3es
9. referral to a urologist for surgical correction
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Question . !. A &'-yr-old boy is noted to ha3e heaturia and proteinuria on a
routine physical eaination. He is without coplaints% and eaination
findings are noral. Results of blood cheistry studies are also noral% but
analysis of the 2!-hr urine specien re3eals 2 g of protein and a noral
creatinine clearance. A renal biopsy is perfored% which re3eals esangial
proliferati3e gloerulonephritis with 3ery bright iunoglobulin A depositsin the esangiu on iunofluorescence. >hich of the following stateents
is true regarding this child?s for of gloerulonephritis@
A0"his disease is ore coon in feales
70"he priary treatent is blood pressure control
C0:rogressi3e 5idney disease occurs in a a1ority ofchildren
80"he copleent C, 3alue is usually low
90Children with this disease rarely present with gross
heaturia
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"he following are recognised presentationsof AR polycystic 5idney disease ecept $
A 7erry aneurys
7 ephrogenic diabetes insipidus
C 7ilateral flan5 asses at birth
8 :resentation with Hypertension
9 :otter?s yndroe
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Question . 6(. A &2-yr-old boy presents with a long-standing history of
polyuria and polydipsia% progressi3e fatigue% decreased appetite%
orningnausea and eesis% weight loss% and ipaired growth 3elocity. n
addition% he
has had no response to a 6-o course of iron therapy for treatent ofaneia.
nitial laboratory e3aluation re3eals 7 of &2( g)d= and seru
creatinine of.* g)d=. 4ther epected laboratory features include all of the
following
ecept$
A09le3ated parathyroid horone le3el
70ncreased anion gap etabolic acidosis
C08ecreased le3els of growth horone
80all% echogenic 5idneys on ultrasonography
90Hypocalceia
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Question . 6. Multicystic dysplastic 5idneys arecharacteriGed by all of the
following ecept$
A0 sually unilateral
70 ncidence of &$2%'''
C0 Autosoal doinant inheritance
80 Most coon neonatal abdoinal ass
90 o function
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"hese features are associated with renal
osteodystrophy ecept $
A increased gut absorption of calciu
7 distal yopathy
C hypophosphataeia8 raised seru al5aline phosphatase
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>hich of the following is characteristic of 7artter?s
yndroe@
&. A3ailable ar5s are shown in brac5ets
2. econdary hyperaldosteronis
,. Hyper5alaeia
!. Metabolic acidosis(. Reduced renal concentrating ability 8iarrhoea
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Question . &2. All of the following gloerulardiseases often anifest with
rapidly progressi3e gloerulonephritis ecept$
A0>egener?s granuloatosis
70ysteic lupus erytheatosus
C0Mebranoproliferati3e gloerulonephritis
80Doodpasture syndroe
90#ocal segental gloerulosclerosis
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A *-day-old infant is hospitaliGed because of lethargy. #indings include$blood pressure% ')!' Hg+ pulse% &!' beats)in+ respiratoryrate% 6' breaths)in+ creatinine% '.6 g)d=+ sodiu%&!' 9L)=+potassiu% (.' 9L)=+ chloride% &'' 9L)=+ bicarbonate% &' 9L)=+blood glucose% F' g)d=+ white blood cell count% &2%''')+noral cerebrospinal fluid+ and urine pH of (.(.
4f the following% the M4" li5ely diagnosis is
A. eningitis
7. organic acideia
C. renal tubular acidosis% type &
8. renal tubular acidosis% type 29. urea cycle defect
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Question . &!. A *-o-old white ale infant presents withfailure to thri3e and
a 7 of *( g)d=. He has a history of a poor urinarystrea. "he ost li5ely
diagnosis is$
A0 Renal artery stenosis
70 Renal hypoplasia
C0 rogenic bladder80 :osterior urethral 3al3es
90 ephrolithiasis
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Question . &'. Cystitis is associated with all
of the following ecept$
A0rgency
70Adeno3irus
C0#e3er
80Absence of renal scarring90eual acti3ity in feales