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101 Cards in this Set

  • Front
  • Back
Addison’s
Disease
Addisonian
Anemia
Albright’s
Syndrome
Alport’s
Syndrome
Alzheimer’s
5.
Argyll-Robertson
Pupil
7.
“Prostitute’s
8.
Pathognomonic
9.
Lesion
Arnold-Chiari
Malformation
Barrett’s
11.
Bartter’s
Syndrome
Becker’s
Muscular
Bell’s
Palsy
Berger’s
Disease
Bernard-Soulier
Disease
Berry
Aneurysm
18.
Often
Bowen’s
Disease
Brill-Zinsser
Disease
Briquet’s
Syndrome
22.
Psychological:
Broca’s
Aphasia
Brown-Sequard
24.
Bruton’s
Disease
Budd-Chiari
26.
Buerger’s
Disease
28.
Seen
Burkitt’s
Lymphoma
30.
8:14
31.
Seen
32.
Starry
Caisson
Disease
Chagas’
Disease
Chediak-Higashi
Disease
36.
Neutropenia,
Conn’s
Syndrome
Cori’s
Disease
Creutzfeldt-Jakob
39.
Crigler-Najjar
Syndrome
41.
Glucuronyl
42.
Less
Crohn’s
43.
44.
(contrast
45.
Clinically:
Curling’s
Ulcer
Cushing’s
47.
48.
Syndrome:
49.
-
Albright’s Syndrome 3. Polyostotic fibrous dysplasia
precocious puberty
Becker’s Muscular Dystrophy 13. Similar to Duchenne
but less severe (mutation
Berger’s Disease 15. IgA nephropathy causing hematuria in kids
usually following infection
Brown-Sequard 24. Hemisection of cord (contralateral loss of pain & temp / ipsilateral loss of fine touch
UMN / ipsi loss of consc.
31. Seen commonly in jaws
abdomen
Chagas’ Disease 34. Trypansoma infection - cardiomegaly with apical atrophy
achlasia
36. Neutropenia
albinism
Cori’s Disease 38. Type III Glycogenosis – Glycogen storage disease (debranching enz: amylo 1
6 glucosidase def. ↑ Glycogen)
Crohn’s 43. IBD; ileocecum
transmural
44. (contrast to UC: limited to colon
mucosa & submucosa
Bell’s Palsy 14. CNVII palsy (entire face
recall that UMN lesion only affects lower face)
Budd-Chiari 26. Post-hepatic venous thrombosis = ab pain
hepatomegaly
Conn’s Syndrome 37. Primary Aldosteronism: HTN
retain Na+ & H2O
Crohn’s 43. IBD
ileocecum, transmural, skip lesions, cobblestones, lymphocytic infiltrate, granulomas
45. Clinically: ab pain & diarrhea
fever
49. - moon face
buffalo hump
Addison’s Disease
1. Primary adrenocortical deficiency
Addisonian Anemia
2. Pernicious anemia (antibodies to intrinsic factor or parietal cells →↓IF →↓Vit B12 →megaloblastic anemia)
Albright’s Syndrome
3. Polyostotic fibrous dysplasia
Alport’s Syndrome
4. Hereditary nephritis with nerve deafness
Alzheimer’s
5. Progressive dementia
Argyll-Robertson Pupil
6. Loss of light reflex constriction (contralateral or bilateral)
Arnold-Chiari Malformation
10. Cerebellar tonsil herniation through foramen magnum = see thoracolumbar meningomyelocele
Barrett’s
11. Columnar metaplasia of lower esophagus (↑risk of adenocarcinoma)- constant gastroesophageal reflux
Bartter’s Syndrome
12. Hyperreninemia
Becker’s Muscular Dystrophy
13. Similar to Duchenne
Bell’s Palsy
14. CNVII palsy (entire face; recall that UMN lesion only affects lower face)
Berger’s Disease
15. IgA nephropathy causing hematuria in kids
Bernard-Soulier Disease
16. Defect in platelet adhesion (abnormally large platelets & lack of platelet-surface glycoprotein)
Berry Aneurysm
17. Circle of Willis (subarachnoid bleed) Anterior Communicating artery
Bowen’s Disease
19. Carcinoma in situ on shaft of penis (↑risk of visceral ca) [compare w/ Queyrat]
Brill-Zinsser Disease
20. Recurrences of rickettsia prowazaki up to 50 yrs later
Briquet’s Syndrome
21. Somatization disorder
Broca’s Aphasia
23. Motor Aphasia (area 44 & 45) intact comprehension
Brown-Sequard
24. Hemisection of cord (contralateral loss of pain & temp / ipsilateral loss of fine touch
Bruton’s Disease
25. X-linked agammaglobinemia (↓B cells)
Budd-Chiari
26. Post-hepatic venous thrombosis = ab pain; hepatomegaly; ascites; portal HTN; liver failure
Buerger’s Disease
27. Acute inflammation of medium and small arteries of extremities →painful ischemia →gangrene
Burkitt’s Lymphoma
29. Small noncleaved cell lymphoma EBV
31. Seen commonly in jaws
abdomen
Caisson Disease
33. Nitric gas emboli
Chagas’ Disease
34. Trypansoma infection - cardiomegaly with apical atrophy
Chediak-Higashi Disease
35. (AR) Phagocyte Deficiency = defect in microtubule polymerization
36. Neutropenia
albinism
Conn’s Syndrome
37. Primary Aldosteronism: HTN; retain Na+ & H2O; hypokalemia (causing alkalosis); ↓renin
Cori’s Disease
38. Type III Glycogenosis – Glycogen storage disease (debranching enz: amylo 1
Creutzfeldt-Jakob
39. Prion infection →cerebellar & cerebral degeneration
Crigler-Najjar Syndrome
40. Congenital hyperbilirubinemia (unconjugated)
Crohn’s
43. IBD; ileocecum
44. (contrast to UC: limited to colon
mucosa & submucosa
Curling’s Ulcer
46. Acute gastric ulcer associated with severe burns
Cushing’s
47. Disease: Hypercorticism 2to ↑ACTH from pituitary (basophilic adenoma)