NPLEX I Flashcards
The femoral artery passes through the adductor hiatus and becomes the _____ artery.
Popliteal
At what level of the cervical plexus does the phrenic nerve arise?
C3-C5
Which vein originates from the dorsal vein of the great toe and empties into the femoral vein?
Great saphenous vein
What is the primary function of the semilunar valves?
Prevents back flow into the ventricles during diastole
The presence of Reed Sternberg cells would be indicative of what diagnosis?
Hodgkin’s lymphoma
Which artery supplies the temporal artery?
External carotid artery
What is the most common cause of congestive heart failure?
Atherosclerosis
Where is Angiotensin-converting enzyme primarily located?
Capillaries of the lungs
The aortic valve is derived from what embryological structure?
Truncus arteriosus
The opening of the left coronary artery is found in what portion of the aortic valve?
Left sinus
Which heart valve is most commonly affected in rheumatic heart disease?
Mitral valve
On which layer of the heart are vegetations found in cases of rheumatic heart disease?
Endocardium
What are the monosaccharides?
Glucose, fructose, galactose, mannose
What are the disaccharides?
Sucrose
Lactose
Maltose
Sucrose is formed by ____.
Glucose + fructose via a1-B2
Lactose is formed by____.
Galactose + glucose via B1-4
Maltose is formed by ____.
Glucose + glucose via a1-4
Pathogenesis and presentation of xeroderma pigmentosum
Defective nucleotide excision repair → inability to repair DNA pyrimidine dimers caused by UV exposure
Presentation: photosensitivity, skin cancer, dry skin
What are the cytoskeletal elements?
Microfilaments: actin, microvilli
Intermediate filaments: desmin, neurofliaments
Microtubules: cilia, flagella, mitotic spindle
Which step in collagen synthesis requires vitamin C?
Hydroxylation - strengthening of the collagen (proline and lysine residues)
Inheritance pattern of osteogenesis imperfecta
Autosomal dominant
Most common gene defect in osteogenesis imperfecta
COL1A1 and COL1A2 - leading to a decrease in the production of otherwise normal type I collagen
Pathogenesis of ehlers-danlos syndrome
Faulty collagen synthesis
Presentation of Ehlers-danlos syndrome
Hyperextensible skin, hypermobile joints, tendency to bleed (easy bruising)