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118 Cards in this Set

  • Front
  • Back
most common cause of amenorrhea
pregnancy
most common cause of pancreatitis
alcohol abuse
most common cause of anemia
iron deficiency
most common cause of nephrotic syndrome in children
minimal change disease
most common cause of nephrotic syndrome in adults
membranous glomerulonephritis
most common cause of osteomyelitis
staph. aureus
most common cause of osteomyelitis in diabetics and sickle cell disease
salmonella
most common cause of osteomyelitis in IV drug users
serratia and pseudomonas
most common cause of constipation
dehydration
most common cause of kidney stones
dehydration
most common cause of pneumonia
strep pneumoniae
most common cause of ascites
alcoholic cirrhosis
most common cause of death
heart disease in US
most common cause of male pseudohermaphrodism
testicular feminization
most common cause of female pseudohermaphrodism
adrenogenital syndrome (congenital adrenal hyperplasia)
most common cause of calf claudication
peripheral vascular disease (PVD)
most common cause of left-sided heart failure
coronary artery disease
most common cause of atherosclerosis
elevated LDL-cholesterol
most common cause of DVT
blood stasis (especially after surgery or late pregnancy)
most common cause of wheezing
asthma
most common cause of a cold in fall/winter
rhinovirus
most common cause of a cold in spring/summer
adenovirus
most common cause of bronchiectasis
cystic fibrosis
most common cause of pleural effusion
CHF
most common cause of pulmonary edema
CHF
most common cause of septic shock
gram (-) bacteria
most common cause of poisoning (in the US)
carbon monoxide
most common cause of iron deficiency at >50 years of age
colon cancer
most common cause of vomiting
viral infection
most common cause of hematemesis
duodenal ulcer
most common cause of hematochezia
diverticulosis
most common cause of melena
duodenal ulcer
most common cause of RLQ pain
appendicitis
most common cause of acute infectious diarrhea
norovirus
most common cause of small bowel obstruction
adhesions
most common cause of erectile dysfunction
diabetes
most common cause of hyperthyroidism
Graves disease
most common cause of hypothyroidism
hashimotos disease
most common cause of yellow CSF (xanthochromia)
bleed in the CNS
most common cause of blindness in the elderly
macular degeneration
most common cause of tremor
essential tremor
most common cause of dementia
alzheimer's disease
most common cause of psychosis
depression
most common cause of headache
tension headache
in cystic fibrosis patients, what is the first bacteria to cause respiratory infections
staph aureus
in cystic fibrosis patients, what bacteria causes respiratory infections after 6 mo
pseudomonas aeruginosa
vitamins that are deficient in cystic fibrosis patients
A, D, E, K
neurotoxic metabolite of phenylalanine that builds up in phenylketonuria
phenyl ketones
sx of a1-antitrypsin deficiency
cirrhosis (from buildup of a1-antitrypsin in hepatocytes) and emphysema (from unregulated elastase damage in lung)
vonGierke is what kind of disease
glycogen storage disease
pompe is what kind of disease
glycogen storage disease
mcardle disease is what kind of disease
glycogen storage disease
sx of glycogen storage diseases
hypoglycemia b/w meals
liver swelling (can store glycogen, but can't utilize it)
hurler is what kind of disease
mucopolysaccharidoses
scheie is what kind of disease
mucopolysaccharidoses
hunter is what kind of disease
mucopolysaccharidoses (X-linked)
sx of mucopolysaccharidoses
corneal clouding and mental retardation (hunter dz has no corneal clouding - hunter's need to see)
niemann-pick is what kind of disease
sphingolipidoses
krabbes is what kind of disease
sphingolipidoses
merachromatic dystrophy is what kind of disease
spingolipidoses
fabry is what kind of disease
sphingolipidoses
gaucher is what kind of disease
sphingolipidoses
tay-sachs is what kind of disease
sphingolipidoses (x-linked)
sx of sphingolipidoses
CNS disorders
inheritance pattern of infant polycystic kidney disease versus adult type
adult: autosomal dominant
infant: autosomal recessive
referred to as bronze diabetes
hemochromatosis
WBC have abnormal microtubules causing multiple recurrent infections
chediak-higashi syndrome
excessive bleeding disease caused by a deficiency in GpIb (platelet to vWF)
bernard-soulier disease
excessive bleeding disease caused by a deficiency in GpIIbIIIa (platelet to platelet)
glanzmanns thromboasthenia
abnormal LDL receptor leading to early atherosclerosis
familial hypercholesterolemia
spherocytosis is due to a defect in what protein
spectrin
what does vWF normally bind to in the serum
GpIb and factor VIII
marfan syndrome is due to a defect in what protein
fibrillin
>6 cafe au lait spots
axillary freckling
von recklinghausen disease (neurofibromatosis 1)
bilateral schwannomas (CNVIII tumors)
hearing deficits
acoustic neurofibromatosis
shagreen's patches (yellow leathering over pre-sacral)
ash leaf patches (hypopigmented leaf like areas)
mental retardation
cysts of liver, pancreas, and kidney
tuberous sclerosis
von-hippel lindau (neurocutaneous syndrome) are at high risk for what disease
renal cell carcinoma
trinucleotide repeat that causes huntington disease (chorea, psychiatric disease, cognitive decline)
CAG
aneurysm present in adults with polycystic kidney disease
berry
factor __ is deficient in hemophilia A
VIII
factor __ is deficient in hemophilia B
IX
inability to eradicate radical O2 species causing hemolysis
G6PD deficiency
triple repeat present in fragile X syndrome
CGG
sphingolipidosis characterized by angiokeratomas (wart-like growths with telangiectasias) and renal failure
fabry disease
deficiency in HGPRT causing excess uric acid and self-mutilation
lesch-nyhan syndrome
lack of dystrophin
duchenne muscular dystrophy
decreased levels of dystrophin
becker muscular dystrophy
low or absent mature B cells
brutons agammaglobulinemia
otitis media
eczema
thrombocytopenia
wiskott-aldrich (IgM dysfunction)
deletion in cri du chat syndrome
5p
deletion in retinoblastoma
13q
deletion in prader willi syndrome
15q11-13 paternal
deletion in angelman syndrome
15q11-13 maternal
HLA type assx with hemochromatosis
HLA A3
HLA type assx with ankylosing spondylitis
B27
HLA type assx with reactive arthritis
B27
HLA type assx with psoriatic arthritis
B27
HLA type assx with narcolepsy
DR2
HLA type assx with multiple sclerosis
DR2
HLA type assx with type I diabetes
DR2 and DR3
HLA type assx with SLE
DR3
HLA type assx with celiac disease
DR3
HLA type assx with rheumatoid arthritis (adult and juvenile)
DR4 DW4 DW14
sacroiliitis
bamboo spine
uveitits
ankylosing spondylitis
conjunctivitis, urethritis, arthritis
reactive arthritis (Reiters) -can't pee, can't see, can't climb a tree
nystagmus
intention tremor
scanning speech
multiple sclerosis
screening and confirmatory tests for lupus
screening: ANA
confirmatory: anti-dsDNA (anti-smith)
false positive test in SLE
VDRL (for lupus due to cardiolipin Ab made)
where is cardiolipin normally found in the body (syphillis membrane molecule)
inner mitochondrial membrane
type of dysphagia present in CREST syndrome
solid and liquid (fibrosis of esophagus, so neuromuscular)
enzyme that is deficient in chronic granulomatous disease
NADPH oxidase
deficient interferon-gamma causing sinopulmonary infections, candidiasis, and cold abscesses
job's syndrome
pharyngeal pouches that fail to develop in DiGeorge syndrome
3rd and 4th
most common infection in SCID
pneumocystis pneumonia
penicillin inhibits what enzyme used in bacterial cell wall synthesis
transpeptidase
penicillin that is not renally excreted (excreted in bile)
nafcillin
pt. who cannot take penicillin are usually give what instead
erythromycin
3rd generation cephalosporin that is not renally excreted (excreted in the bile)
ceftriaxone