• Shuffle
    Toggle On
    Toggle Off
  • Alphabetize
    Toggle On
    Toggle Off
  • Front First
    Toggle On
    Toggle Off
  • Both Sides
    Toggle On
    Toggle Off
  • Read
    Toggle On
    Toggle Off
Reading...
Front

Card Range To Study

through

image

Play button

image

Play button

image

Progress

1/118

Click to flip

Use LEFT and RIGHT arrow keys to navigate between flashcards;

Use UP and DOWN arrow keys to flip the card;

H to show hint;

A reads text to speech;

118 Cards in this Set

  • Front
  • Back
Abdominal pain, ascites,hepatomegaly
budd-chiari syndrome (post-hepatic venous thrombosis)
achilles tendon xanthoma
familial hypercholesterolemia (decreased LDL receptor signaling)
Adrenal hemorrhage, hypotension, DIC
Waterhouse-Friderichsen syndrome (meningococcemia)
Arachnodactyly, lens dislocation, aortic dissection, hyperflexible joints
Marfan's syndrome (fibrillin defect)
athlete with polycythemia
2ndary to EPO injection
back pain, fever, night sweats, weight loss
Pott's disease (vertebral tuberculosis)
bilateral hilar lymphadenopathy, uveitis
sarcoidosis (noncaseating granulomas)
blue sclera
osteogenesis imperfecta
bluish line on gingiva
burton's line (lead poisoning)
bone pain, bone enlargement, arthritis
Paget's dz of bone (increased osteoblastic and osteoclastic activity)
bounding pulses, diastolic heart murmur, head bobbing
aortic regurgitation
"butterfly" facial rash and Raynaud's phenomenon in a young female
SLE
cafe-au-lait spots, lisch nodules (iris hamartomas)
NF1 (+pheochromocytoma, optic glioma)
cafe-au-lait spots, polyostotic fibrous dysplasia, precocious puberty, multiple endocrine abnormalities
McCune-Albright syndrome (mosaic G-protein signaling mutation)
Calf pseudohypertrophy
muscular dystrophy (most commonly Duchenne's): X-linked recessive deletion of dystrophin gene
cherry red spot on macula
Tay-Sachs (ganglioside accumulation) or Niemann-Pick (sphingomyelin accumulation) or central retinal artery occlusion
Chest pain on exertion
angina (stable: with moderate exertion; unstable: with minimal exertion)
Chest pain, pericardial effusion/friction rub, persistent fever following MI
Dressler's syndrome (autoimmune-mediate post-MI fibrinous pericarditis, 1-12 weeks after acute episode)
Child uses arms to stand up from squat
gower's sign (Duchenne muscular dystrophy)
Child with fever later develops red rash on face that spreads to body
"slapped cheeks" (erythema infectiousum/fifth disease: parvovirus B19)
chorea, dementia, caudate degeneration
Huntington's disease (autosomal dominant CAG repeat expansion)
chronic exercise intolerance with myalgia, fatigue, painful cramps, myoglobinuria
McArdle's Disease (muscle glycogen phosphorylase deficiency)
cold intolerance
hypothyroidism
conjugate lateral gaze palsy, horizontal diplopia
internuclear opthalmoplegia (damage to MLF; bilateral-multiple sclerosis, unilateral-stroke)
continuous "machinery" heart murmur
PDA (close with indomethacin; open or maintain with misoprostol)
cutaneous/dermal edema due to CT disorder
myxedema (caused by hypothyroidism, Grave's disease (pre-tibial))
dark purple skin/mouth nodules
Kaposi's sarcoma (usually AIDS pts[MSM]: associated with HIV)
deep labored breathing/hyperventilation
Kussmaul breathing (diabetic ketoacidosis)
dermatitis, dementia, diarrhea
Pellagra (niacin [vitamin B3] deficiency)
dilated cardiomyopathy, edema, alcoholism or malnutrition
wet beriberi (thiamine [vitamin B1] deficiency)
dog or cat bite resulting in infection
Pasteurella multocida (cellulitis and injection site)
dry eyes, dry mouth, arthritis
Sjogren's syndrome (autoimmune destruction of exocrine glands)
dysphagia (esophageal webs), glossitis, iron deficiency anemia
Plummer-Vinson syndrome (may progress to esophageal squamous cell carcinoma)
elastic skin, hypermobility of joints
Ehlers-Danlos syndrome (type III collagen defect)
enlarged hard left supraclavicular node
Virchow's node (abdominal mets)
erythroderma, lymphadenopathy, hepatosplenomegaly, atypical T cells
Sezary syndrome (cutaneous T cell lymphoma) OR mycosis fungoides
facial muscle spasm upon tapping
chvostek's sign (hypocalcemia)
fat, female, forty, fertile
cholelithiasis (gallstones)
fever, chills, headache, myalgia following treatment for syphilis
Jarisch-Herxheimer reaction (rapid lysis of spirochetes results in toxin release)
fever, cough, conjunctivitis, coryza, diffuse rash
measles (morbillivirus)
fever, night sweats, weight loss
B symptoms (staging) of Lymphoma
fibrous plaques in soft tissue of penis
peyronie's disease (CT disorder)
gout, mental retardation, self-mutilating behavior in boy
lesch-nyhan syndrome(HGPRT deficiency, X-linked recessive)
green-yellow rings around peripheral cornea
kayser-fleischer rings (copper accumulation from Wilson's Disease)
hamartomatous GI polyp, hyperpigmentation of mouth/feet/hands
Peutz-Jeghers syndrome (inherited, benign polyposis can cause bowel obstruction, increased cancer risk, mainly GI)
HSM, osteoporosis, neurologic symptoms
Gaucher's Disease (glucocerebrosidase deficiency)
Herediatry nephritis, sensorineural hearing loss, cataracts
Alport syndrome (mutation in alpha chain of collagen IV)
hyperphagia, hypersexuality, hyperorality, hyperdocility
Kluver-Bucy syndrome (bilateral amygdala lesion)
hyperreflexia, hypertonia, Babinskin sign present
UMN damage
hyporeflexia, hypotonia, atrophy, fasciculations
LMN damage
hypoxemia, polycythemia, hypercapnia
"blue bbloater" (chronic bronchitis: hyperplasia of mucous cells)
indurated ulcerated genital lesion
nonpainful: chancre (primary syphilis,via Treponema pallidum)painful: chancroid (Haemophilus ducreyi)
infant with: cleft lip/palate, microcephaly, holoprosencephaly, polydactyly cutis aplasia
Patau's syndrome (trisomy 13)
infant with: failure to thrive, hepatosplenomegaly, neurodegeneration
Niemann-Pick Disease (genetic sphingomyelinase deficiency)
Infant with:hypoglycemia, failure to thrive, hepatosplenomegaly
Cori's Disease (debranching enzyme deficiency)
Infant with: microcephaly, rocker-bottom feet, clenched hand, structural heart defect
Edward's syndrome (trisomy 18)
jaundice, palpable distended non-tender gallbladder
Courvoisier's sign (distal obstruction of the biliary tree)
large rash with bull's eye appearance
erythema chronicum migrans from Ixodes tick bite (Lyme disease: Borrelia)
lucid interval after traumatic brain injury
Epidural hematoma (middle meningeal artery rupture)
male child, recurrent infections, no mature B cells
Bruton's disease (X-linked agammaglobulinemia)
mucosal bleeding and prolonged bleeding time
Glanzmann's thrombasthenia (defect in platelet aggregation due to lack of Gp IIb/IIIa)
muffled heart sounds,distended neck veins,hypotension
Beck's triad of cardiac tamponade
multiple colon polyps, osteomas/soft tissue tumors, impacted/supernumerary teeth
Gardner's syndrome (subtype of FAP)
myopathy (infantile hypertrophic cardiomyopathy), exercise intolerance
Pompe's dz(lysosomal alpha-1,4-glucosidase deficiency)
neonate with arm paralysis following difficult birth
Erb-Duchenne palsy (superior trunk [C5-C6} brachial plexus injury: "waiter's tip"
no lactation postpartum, absent menstruation, cold intolerance
Sheehan's syndrome (pituitary infarction)
nystagmus, intention tremor, scanning speech, bilateral internuclear opthalmoplegia
multiple sclerosis
oscillating slow/fast breathing
cheyne-stokes respirations (central apnea in CHF or increased intracranial pressure)
painful blue fingers/toes, hemolytic anemia
cold-agglutinin disease (AI hemolytic anemia caused by Mycoplasma pneumoniae, infectious mononucleosis)
Painful, pale, cold fingers
Raynaud's phenomenon (vasospasm in extremities)
Painful, raised red lesions on pad of fingers/toes
Osler's node (infective endocarditis, immune complex deposition)
Painless erythematous lesions on palms and soles
Janeway lesions (infective endocarditis, septic emobli/microabscesses)
Painless jaundice
cancer of the pancreatic head obstructing bile duct
palpable purpura on buttocks/legs, joint pain, abdominal pain (child), hematuria
Henoch-Schonlein purpura (IgA vasculitis affecting skin and kidneys)
pancreatic, pituitary, parathyroid tumors
MEN1 (autosomal dominant)
periorbital and/or peripheral edema, proteinuria, hypoalbuminemia, hypercholesterolemia
Nephrotic Syndrome
pink complexion, dyspnea, hyperventilation
"pink puffer" (emphysema: centriacinar [smoking], panacinar [alpha1-antitrypsin deficiency])
polyuria, renal tubular acidosis type II, growth failure, electrolyte imbalances, hypophosphatemic rickets
Fanconi's syndrome (proximal tubular reabsorption defect)
positive anterior "drawer sign"
anterior cruciate ligament injury
pruritic, purple, polygonal planar papules and plaques (6 P's)
Lichen planus
ptosis, miosis, anhidrosis
Horner's Sydrome (sympathetic chain lesion)
pupil accommodates but doesn't react
Argyll-Robertson pupil (neurosyphilis)
rapidly progressive leg weakness that ascends following GI/upper respiratory infection
Guillain-Barre syndrome (acut autoimmun inflammatory demyelinating polyneuropathy)
rash on palms and soles
Coxsackie A, 2ndary syphilis, Rocky Mountain spotted fever
recurrent colds, unusual eczema, high serum IgE
Hyper-IgE syndrome (Job's syndrome: neutrophil chemotaxis abnormality)
Red "currant jelly" sputum in alcoholic or diabetic patients
Klebsiella pneumoniae
red "currant jelly" stools
acute mesenteric ischemia (adults), intussusception (infants)
Red, itchy, swollen rash of nipple/areola
Paget disease of the breast (sign of underlying neoplasm)
Red urine in the morning, fragile RBCs
Paroxysmal nocturnal hemoglobinuria
Renal cell carcinoma (bilateral), hemangioblastomas, angiomatosis, pheochromocytoma
von Hippel-Lindau disease (dominant tumor suppressor gene mutation)
Resting tremor, rigidity, akinesia, postural instability
Parkinson disease (nigrostriatal dopamine depletion)
Retinal hemorrhages with pale centers
Roth spots (bacterial endocarditis)
Severe jaundice in neonate
Crigler-Najjar syndrome (congenital unconjugated hyperbilirubinemia)
Severe RLQ pain with palpation of LLQ
Rovsing sign (acute appendicitis)
Severe RLQ pain with rebound tenderness
McBurney sign (acute appendicitis)
Short stature,  incidence of tumors/leukemia, aplastic anemia
Fanconi anemia (genetic loss of DNA crosslink repair; often progresses to AML)
Single palmar crease
Down syndrome
Situs inversus, chronic sinusitis, bronchiectasis, infertility
Kartagener syndrome (dynein arm defect affecting cilia)
Skin hyperpigmentation, hypotension, fatigue
Addison disease (1° adrenocortical insufficiency causes ACTH and  α-MSH production)
Slow, progressive muscle weakness in boys
Becker muscular dystrophy (X-linked missense mutation in dystrophin; less severe than Duchenne)
Small, irregular red spots on buccal/lingual mucosa with blue-white centers
Koplik spots (measles; rubeola virus)
Smooth, flat, moist, painless white lesions on genitals
Condylomata lata (2° syphilis)
Splinter hemorrhages in fingernails
Bacterial endocarditis
"Strawberry tongue"
Scarlet fever, Kawasaki disease, toxic shock syndrome
Streak ovaries, congenital heart disease, horseshoe kidney, cystic hygroma at birth, short stature, webbed neck, lymphedema
Turner syndrome (45,XO)
Sudden swollen/painful big toe joint, tophi
Gout/podagra (hyperuricemia)
Swollen gums, mucosal bleeding, poor wound healing, petechiae
Scurvy (vitamin C deficiency: can't hydroxylate proline/lysine for collagen synthesis)
Swollen, hard, painful finger joints
Osteoarthritis (osteophytes on PIP [Bouchard nodes], DIP [Heberden nodes])
Systolic ejection murmur (crescendo-decrescendo)
Aortic valve stenosis
Thyroid and parathyroid tumors, pheochromocytoma
MEN 2A (autosomal dominant RET mutation)
Thyroid tumors, pheochromocytoma, ganglioneuromatosis
MEN 2B (autosomal dominant ret mutation)
Toe extension/fanning upon plantar scrape
Babinski sign (UMN lesion)
Unilateral facial drooping involving forehead
Facial nerve (LMN CN VII palsy)
Urethritis, conjunctivitis, arthritis in a male
Reactive arthritis associated with HLA-B27
Vascular birthmark (port-wine stain)
Sturg-Weber check
Vomiting blood following gastroesophageal lacerations
Mallory-Weiss syndrome(alcoholic and bulimic patients)
Weight loss, diarrhea, arthritis, fever, adenopathy
Whipple disease (Tropheryma whipplei)
"Worst headache of my life"
Subarachnoid hemorrhage