Sandbox:khurram: Difference between revisions
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! colspan="1" rowspan="1" style="background: #4479BA; color: #FFFFFF; text-align: center;" |Symptom 2 | ! colspan="1" rowspan="1" style="background: #4479BA; color: #FFFFFF; text-align: center;" |Symptom 2 | ||
! style="background: #4479BA; color: #FFFFFF; text-align: center;" |Symptom 3 | ! style="background: #4479BA; color: #FFFFFF; text-align: center;" |Symptom 3 | ||
! style="background: #4479BA; color: #FFFFFF; text-align: center;" | | ! style="background: #4479BA; color: #FFFFFF; text-align: center;" |Skin necrosis | ||
! colspan="1" rowspan="1" style="background: #4479BA; color: #FFFFFF; text-align: center;" |Physical exam 2 | ! colspan="1" rowspan="1" style="background: #4479BA; color: #FFFFFF; text-align: center;" |Physical exam 2 | ||
! style="background: #4479BA; color: #FFFFFF; text-align: center;" |Physical exam 3 | ! style="background: #4479BA; color: #FFFFFF; text-align: center;" |Physical exam 3 |
Revision as of 19:48, 20 August 2018
Editor-In-Chief: C. Michael Gibson, M.S., M.D. [1] Associate Editor(s)-in-Chief:
Differentiating [disease name] from other diseases on the basis of [symptom 1], [symptom 2], and [symptom 3]
On the basis [symptom 1], [symptom 2], and [symptom 3], [disease name] must be differentiated from [disease 1], [disease 2], [disease 3], [disease 4], [disease 5], and [disease 6].
Diseases | Clinical manifestations | Para-clinical findings | Gold standard | Additional findings | |||||||||||||
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
Symptoms | Physical examination | ||||||||||||||||
Lab Findings | Imaging | Histopathology | |||||||||||||||
Symptom 1 | Symptom 2 | Symptom 3 | Skin necrosis | Physical exam 2 | Physical exam 3 | Platelet count | Bleeding time | PT | PTT | Peripheral blood smear | Imaging 1 | Imaging 2 | Imaging 3 | ||||
Antithrombin deficiency | |||||||||||||||||
Factor V Leiden mutation | |||||||||||||||||
Protein C deficiency | |||||||||||||||||
Protein S deficiency | |||||||||||||||||
Prothrombin gene mutation | |||||||||||||||||
von Willebrand disease | Ristocetin cofactor assay | ||||||||||||||||
DIC | |||||||||||||||||
Antiphospholipid antibody syndrome |