290 results
Wellen's Syndrome 
Type A - Biphasic T wave 
Type B - Deeply inverted T wave
Wellen's Syndrome ... specific for a critical ... intervention #Wellens #Syndrome ... #TypeA #TypeB # ... Electrocardiogram #Diagnosis
Dermatologic Extraintestinal Manifestations in IBD - IBD Algorithm

Erythema Nodosum
Pyoderma Gangrenosum
Metastatic Crohn's Disease
Sweet Syndrome
EBA

Dr. Wade Billings @wabillin

#Dermatologic
Dermatologic Extraintestinal ... Metastatic Crohn's Disease ... Sweet Syndrome ... @wabillin #Dermatologic ... #diagnosis
Mucous Membrane Disorder - Differential Diagnosis Algorithm
Erosions/Ulcers/Blisters
 - Primary Dermatologic Diseases
     •
- Differential Diagnosis ... Blisters - Primary Dermatologic ... Stevens-Johnson Syndrome ... • Behcet's syndrome ... #Differential #Diagnosis
Cutaneous Manifestations of Monoclonal Gammopathy
 • Extravascular lg Deposits: Systemic amyloidosis, Nodular amyloidosis, Macroglobulinoderma, Follicular hyperkeratotic
Intravascular lg deposits: Type ... Autoantibody activity: Type ... Cold agglutinin disease ... manifestations #dermatology ... #skin #clinical
Tweetorial - Stevens Johnson Syndrome (SJS)

By Dr. Steven Chen @DrStevenTChen

#StevensJohnsonSyndrome #SJS #Dermatology #Diagnosis #Tweetorial #Pathphysiology
Stevens Johnson Syndrome ... StevensJohnsonSyndrome #SJS #Dermatology ... #Diagnosis #Tweetorial ... #Pathphysiology
Staphylococcal Scalded Skin Syndrome (SSSS) 
(aka Ritter disease)

#Staphylococcal #Scalded #Skin #Syndrome #SSSS #Diagnosis #Pediatrics #Dermatology #Ritter
(aka Ritter disease ... Scalded #Skin #Syndrome ... #SSSS #Diagnosis ... #Pediatrics #Dermatology ... #Ritter #Disease
Ashkenazi Jewish Genetic Screening Algorithm
 • Bloom syndrome
 • Canavan disease
 • Familial dysautonomia
 • Fanconi
Algorithm • Bloom syndrome ... syndrome type 2 ... syndrome type 1F ... • Usher syndrome ... Screening #Algorithm #diagnosis
Causes of Hypercalcemia
Parathyroid hormone–dependent
Primary hyperparathyroidism
Familial hypocalciuric hypercalcemia
Lithium-associated
Tertiary hyperparathyroidism
Genetic disorders (e.g., multiple endocrine neoplasia type 1 or
endocrine neoplasia type ... 1 or type 2A, familial ... Granulomatous disease ... - Williams syndrome ... #Differential #Diagnosis
Causes of Hypocomplementemia - CHAMPS Mnemonic
C - Cryoglobulinemia (85%), C3 glomerulopathy, cirrhosis
H - Heavy Chain deposition
Chain deposition disease ... antiphospholipid syndrome ... 1 (50%-80%), type ... CHAMPS #Mnemonic #diagnosis ... #differential #hematology
Hepatorenal Syndrome Diagnosis
 • ↑ in serum Cr of ≥ 0.3mg/dL above baseline
Hepatorenal Syndrome ... Diagnosis • ↑ ... • Severe liver disease ... #Hepatorenal #Syndrome ... #diagnosis #HRS