3rd BIMONTHLY RECALLS Flashcards
What is the most common cause
of acute renal failure in
children?
a. Hemolytic-Uremic Syndrome
b. Henoch-Schonlein Purpura
Nephritis
c. Goodpasture Syndrome
d. Chronic Tubulointerstitial
Nephritis
a. Hemolytic-Uremic Syndrome
Chronic granulomatous disease
shows the following clinical
features EXCEPT:
a. Dermatitis
b. Otitis media
c. Acute suppurative infection
d. Hepatomegaly with abscess
c. Acute suppurative infection
This syndrome is caused by
mutations in the PTX2
transcription gene.
a. Hall-Pallister syndrome
b. Hypogammaglobulinemia
c. Reiger syndrome
d. Ritter’s syndrome
c. Reiger syndrome
One of the following is associated
with increased risk of developing
chronic uveitis among children
with JRA?
a. ANA titer
b. Rheumatoid factor
c. Elevated ESR, CRP
d. Hypergammaglobulinemia
a. ANA titer
A life threatening form of
hemophagocytic lymphohistiocytosis is commonly associated with this deficiency.
a. Chediak Higashi Syndrome
b. Leukocyte Adhesion Defect
c. Wisckott Aldrich Syndrome
d. Severe Combined
Immunodeficiency
a. Chediak Higashi Syndrome
One of the following laboratory
parameters is specific for SLE in
children:
a. ANA
b. Anti-dsDNA
c. ANti-Smith antibody
d. C-reactive proteins
c. ANti-Smith antibody
Mutations in this gene cause
septo-optic dysplasia:
a. HESX1
b. LHX3
c. LHX4
d. PTX2
a. HESX1
The initial single most important
laboratory test for a child with
short stature is
a. CBC
b. urinalysis
c. Serum electrolytes
d. x-ray of L hand for bone aging
d. x-ray of L hand for bone aging
Shawl sign is seen in which of the
following rheumatic diseases of
childhood?
a. Juvenile dermatomyositis
b. Henoch-Schِnlein purpura
c. Systemic lupus
erythematosus
d. Systemic-onset juvenile
idiopathic arthritis
a. Juvenile dermatomyositis
Rita, an 11-year-old female with history of fatigue, malaise, and progressive muscle weakness, accompanied by low-grade fevers and scaly, red plaques are found across the knuckles, she is not able to sit up from a supine
position. Laboratory exams showed elevated muscle enzymes (ALT, AST, LDH, CPK, and aldolase), EMG abnormalities: fasciculations, needle insertion irritability, and high-frequency discharges. What do you think is the complication for this disease?
a. calcinosis
b. infections
c. avascular necrosis
d. myocardial infarction
a. calcinosis
One of the following is not a
minor criteria in the diagnosis of
Juvenile Systemic Sclerosis:
a. Hepatomegaly
b. Right sided heart failure
c. Gastroesophageal reflux
d. Pulmonary hypertension
a. Hepatomegaly
Linear IgG on immunofluorescence is found in this particular renal disease that manifests as acute glomerulonephritis.
a. Ig A Nephropathy
b. Goodpasture Syndrome
c. Poststreptococcal Glomerulonephritis
d. Rapidly Progressive Glomerulonephritis
b. Goodpasture Syndrome
The rheumatic diseases of
childhood are characterized by
autoimmunity and inflammation,
which may be localized or
generalized. Which of the
following is the classical rheumatic
disease of childhood :
a. Scleroderma
b. Bechet syndrome
c. Juvenile rheumatoid arthritis
d. Sjogren syndrome
c. Juvenile rheumatoid arthritis
Definitive diagnosis of short
stature is the provocative test.
One of the following is not
included :
a. Insulin
b. arginine
c. leucine
d. glucagon
c. leucine
Bruton tyrosine kinase protein is
commonly associated with this
type of immunodeficiency.
a. Chediak Higashi Syndrome
b. Leukocyte Adhesion Defect
c. Chronic Granulomatous
Disease
d. X-linked Agammaglobulinemia
d. X-linked Agammaglobulinemia