UWORLD Q Flashcards
Which type of HLA is associated with Ankylosing sondylitis?
HLA-B27
HLA Class I Serotype
What neurotransmitter is important in the development of tolerance to morphine?
Glutamate
Fluid accumilation around the testical in a 5 month old infant is indicative of this kind of hernia
Indirect Hernia–> collection of fluid within the tunica vagnialis and hydrocoele
In which part of the nephron would PAH be lowest? Why?
In Bowman’s space.
PAH is filtered and secreted. The secretion takes place in the proximal tubule. Therefore the lowest concentration of PAH woul dbe up stream of that (Bowman’s space)
Young child of European descent with fair skin, light eyes, and musty or mousy ordor. (Also may see mental status changes)
What AA becomes essential? What enzyme is implicated?
Phenylketonuria (PKU)
Lack of phenylalanine hydroxylase causes a build up of phynylalanine with a lack of conversion to tyrosine.
Tyrosine becomes essential. Leads to a lck of pigment production and catecholamine production.

Two common side effects of statin therapy, elevation of what kinase is commonly seen?
Hepatic toxicity
Myopathy–> Creatine Kinase elevation
47XXY
What does this person look like?
What is the name of the Syndrome?
Kleinfelter Syndrome
Tall, Gynecomastia, Infertile
What is the major important step in gluconeogenisis?
Oxaloacetate –> Phophoenolpyruvate
Malate–>oxaloacetate–> Phophoenolpyruvate (by phosphoenolpyruvate carboxikinase [PEPCK])

15 y/o pt. with a low fever, cough and sore throat. What is the name of the cell seen on peripheral blood smear? What kind of cell is it?

Downey cell–> infection with EBV (infectous mononucleosis)
Proliferation of atypical CD8+ T-lymphocytes
Equation for net excretion of Substance A=
Net Excretion of Substance A= (inulin clearance)(Plasma concentration of substance A) - (tubular reabsorption of substance A)
Calculation of filtration of substance A?
Filtration of A= (inulin clearence)(Plasma concentration of A)
What interleukin is release from what cell in excess in chronic asmatic bronchiolitis?
IL-5 from Th2 helper cells–> activates eosinophils
–> leads to the excess release of eosinophilic granules–> **Charcot-leyden chrystals **
Infant’s urine is brought in and had turned dark or black on the way to the office. What is the disorder? What enzyme deficiency?
Alkaptonuria
Inadequate conversion of Tyrosine to fumerate by homogentisate 1,2-deoxygenase
Leads to a build up of homogentisic acid and onchronosis (dark pigment deposistion at mucos membranes)

This image is indicative of what disease? Why?
What other signs may this patient have?
What is the mode of inheritance of this disease?
Neurofibromatosis Type 1
Multiple cafe-au-lait spots and neurofibromas. This patient may also experience arthralgias, vision changes and headaches
-Autosomal dominant single gene inheritance of NF1 gene on chromosome 17
Medication used to help diagnose asthma in a patient
Methacholine Challenge (muscarinic agonist)
Decrease of FEV1 of more than 20%
Young child with tonsilar exudates that stain with aniline dye (methylene blue)?
What is the mechanism of pathogenisis of this organsim?
Cornybacterium diptheriae
(G+ polymorphic chinese letters on microscopy)
AB toxin- B gains access and A subunit inhibits protein synthesis by binding to EF-2 of ribosomes.
Which virus type (enveloped or non-enveloped) is sensitive to the action of ether and other organic solvents? Why?
Enveloped
The envelope is derived from the host’s lipid bilayer membrane and is disrupted by the ether–> loss of infectivity
Which Gp is important for the binding of platelets to vWF and the underlying collagen?
Which Gp is involved in platelet aggregation? Which moniclonal antibody blocks this function? How?
- GpIb is responsible for initial binding of platelets to the underlying collagen. This binding activates the release of ADP(clopidigrel) and thromboxane A2 (aspirin) to activate other platelets.
- GpIIb/IIIa is responsible for platelet aggregation. Multiple IIb/IIIa receptors are cross linked by fibrinogen and this function is blocked by drugs like abciximab.
What race female has a higher bone desity at similar ages?
Black female
A defect in debranching enzyme presents how?
What is the name for this disorder?
What is the normal function of the enzyme defect?
Cori disease (debranching enzyme defect) presents with:
–> hepatomegaly, hypoglycemia, hypertiglyceridemia, and ketoacidosis.
Debranching enzyme–> normally cleaves the last 3 or 4 glycogen at their alpha 1-4 linkages and moves them to the main chain. Then the alpha-1,6-glucosidase cleaves the last glycogen to liberate glucose.
McArdel’s Disease
Deficiency of Glycogen Phosphorylase in muscle (McArdel’s=Muscle)
–> increased glycogen in the muscles with no breakdown leading to painful muscle cramps and myoglobinuria with exercise
Pompe’s Disease
Deficiency of lysosomal alpha-1,4-glocosidase (normally cleaves glycogen A-1,4-glycocidic bonds)
–> Leads to a buildup of glycogen in all tissues but notably the heart leading to cadiomegaly.
(Pompe= buildup in the Pump)
Von-Gierke’s disease
Lack of Glucose-6-phosphatase dosen’t allow of liberation of glucose after the final step of glycogenolysis or gluconeogenisis.
Results in: severe fasting hypoglycemia, Marked increase in liver glycogen, increased blood lactate and hepatomegaly.
What antibody is present in high amounts and is very specific for RA?
Anti-cyclic citrullinated peptide antibodies (Anti-CCP)








