NMBE 13 practice test Flashcards

1
Q

Scleroderma in regards to esophagus and LES tone (increase/decrease)?

A

Decreased esophageal peristalsis Decreased lower esophageal sphincter tone

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2
Q

Warfarin overdose treatment (both mild and severe)

A

In mild cases, can be treated with Vitamin K (delayed response, need to generate more. In severe cases, can be treated with fresh frozen plasma (much more rapid)

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3
Q

Chronic transplant rejection mediated by CD8+ T cells is due to….

A

Direct cytotoxicity to graft cells

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4
Q

clostridium tetani mechanism

A

A protease that cleaves SNARE –>inhibits inhibitory neurotransmitter (glycine, GABA) release from Renshaw cells in spinal cord leading to spasticity (opisthotonos, trismus)

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5
Q

The presence of _____ aids the bacteria in adhering to the urinary tract epithelium and withstanding the urine flow

A

adhesions (pilli)

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6
Q

Heteroplasmy

A

A cell can have some mitochondria that have a mutation in the mtDNA and some that do not (variable expression in mitochondrial inherited diseases) I.E. mother has 50% mutation and then daughters and sons have 100% mutation

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7
Q

Placenta Accreta

A

all or part of the placenta adheres abnormally to the myometrium Accreta – chorionic villi attach to the myometrium, rather than being restricted within the decidua basalis. Leads to an increase in heavy bleeding when vaginal birth is attempted

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8
Q

Schizoid

A

does not like being with people, prefers individual activities, indifferent to sexual behavior SchizoiD=Distant

Key in diagnosis is that it causes social or occupational dysfunction (lots of people can be weird, but it needs to interfere with daily life to be diagnosed)

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9
Q

avoidant personality

A

Hypersensitive to rejection, socially inhibited, timid, feelings of inadequacy, desires relationships with others (vs. schizoid)

-biggest difference from schitzoid is that avoidant pts WANT to interact with people

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10
Q

Celiac disease is associated with what condition

A

Dermatitis Herpetiformis -Pruritic papules, vesicles, and bullae (often found on elbows

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11
Q

Pemphigus vulgaris

A

Potentially fatal autoimmune skin disorder with IgG antibody against desmoglein 1 and desmoglein 2 (component of desmosomes that link together squamous cells of the epidermis). Nikolsky sign + (separation of epidermis upon manual stroking of skin)

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12
Q

Lesch Nyhan Syndrome (what is absent, what are pathways affected, what is produced more, what are sx)

A

Defective purine salvage, owing to absence of HGPRT

Hypoxanthine –> IMP

Guanine –> GMP

Results in excessive uric acid production and de novo purine synthesis -self mutilation behavior, hyperuricemia, gout, aggression

tx: allopurinol (xanthine oxidase inhibitor), which makes sense since cannot recycle the purines, produce more urea down the line.

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13
Q

Crescendo-Decrecendo heart murmur

A

Aortic Stenosis Systolic murmur following ejection click Often due to aggravated calcific aortic stenosis or bicuspid aortic valve Can lead to: syncope, angina, dyspnea on exertion (SAD)

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14
Q

Acute intermittent porphyria

A

AD Porphobilinogen deaminase is defective enzyme Symptoms (5 P’s):

  1. Painful abdomen
  2. Port wine–colored urine
  3. Polyneuropathy
  4. Psychological disturbances
  5. Precipitated by drugs (e.g., cytochrome P-450 inducers), alcohol, starvation
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15
Q

Ventricular Septal Defect murmur

A

holosystolic harsh sounding murmur. Loudest at tricuspid area most common congenital cardiac defect

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16
Q

Lambert Eaton = Myasthinic Syndrome

A

Antibodies to calcium channels at presynaptic terminal Results in proximal muscle weakness when less ACh released improves with muscle use because Calcium eventually work its way into presynaptic terminal Associated with small cell lung cancer

17
Q

Hunter Syndrome

A

Mild Hurler + aggressive behavior, no corneal clouding. Iduronate sulfatase deficiency XLR (boys hunt, eyes are clear to hunt)

18
Q

Hurler Syndrome

A

Autosomal Recessive developmental delay, gargoylism, airway obstruction, corneal clouding, hepatosplenomegaly

-α-l-iduronidase deficiency

NOT X-Linked!

19
Q

Interleukin 1 (secreted by macrophages)

A

Also called osteoclast activating factor endogenous pyrogen, causes fever and acute inflammation. Activates endothelium to express adhesion molecules

20
Q

Gilbert Syndrome

A

caused by UDP gluconyl transferase deficiency (converting UCB –> CB in liver) increased unconjugated bilirubin without overt hemolysis. Bilirubin with fasting and stress VERY common and usually asymptomatic

21
Q

Type 2 error (beta)

A

Says there is not an effect or difference when in fact there is. =false negative error power and type 2 errors are inversely proportional (increase sample size, precision of measurement, decrease chance for type 2 error)

22
Q

Japanese food leads to increased risk of what and why?

A

gastric cancer due to increased nitrosamines in smoked foods

23
Q

elbow flexion done by what muscles and innervated by what nerve?

A

biceps and brachialis both innervated by musculocutaneous nerve

24
Q

Minimal Change Disease

A

most common form of nephrotic syndrome characterized by 2+ protein in urine, puffy eyes, no red cell casts -Usually found in children Often 1° (idiopathic) and may be triggered by recent infection, immunization, immune stimulus. Rarely, may be 2° to lymphoma See effacement of the foot processes and loss of negative glomerular charge (changes seen on EM, normal on Light microscope)

In children 1-10 years who do not have hypertension, gross hematuria, renal failure, extra-renal symptoms such as rashes or purpura, or low complement levels it is reasonable to start therapy with prednisone without obtaining a renal biopsy

25
Q

Atrophy mechanism (2)

A
  1. decreased protein synthesis 2. increased protein degradation