214 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
Lactic Acidosis - Classification and Differential Diagnosis
Type A Lactic Acidosis: Inadequate Oxygen Delivery
 • Anaerobic muscular
and Differential Diagnosis ... with underlying disease ... failure, Short bowel syndrome ... Carbon monoxide, Cyanide ... #Differential #Diagnosis
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
Hepatorenal Syndrome Diagnosis
 • ↑ in serum Cr of ≥ 0.3mg/dL above baseline
Hepatorenal Syndrome ... Diagnosis • ↑ ... • Severe liver disease ... #Hepatorenal #Syndrome ... #diagnosis #HRS
Vertebral Body Abnormalities

A sheet of common (and uncommon) vertebral body findings, because a completely “normal” spine
Vertebra Hurler Syndrome ... Morquio Syndrome ... Neurofibromatosis Type ... Anomalies #Spine #Diagnosis ... #Vertebrae #diseases
Cystic Lung Disease
Upper Lobe Predominant: 
Langerhans Cell Histiocytosis, Pneumocystis Jiroveci, Hypersensitivity Pneumonitis, Neurofibromatosis Type 1, Paracoccidioidomycosis,
Neurofibromatosis Type ... Ehlers-danlos Syndrome ... Amyloidosis, Proteus Syndrome ... Birt-Hogg-Dubé Syndrome ... #differential #diagnosis
Lactic Acidosis - Overview and Pathophysiology
Lactic acid is an endogenous substrate for gluconeogenesis, that is constantly
- Overview and Pathophysiology ... of underlying disease ... PLUS a pH < 7.35 TYPE ... #differential #diagnosis ... #pathophysiology
Gaucher Disease 

Pathophsiology
 • Lysosomal storage disorder
 • Deficiency of ß-glucocerebrosidase
• Accumulation of glucosylceramide in macrophages
Diagnosis
Gaucher Disease ... Pathophsiology ... in GBA1 gene Clinical ... Neurological involvement (type ... #Diagnosis #Signs
Cryoglobulinemia Summary

Cryoglobulins:
 • Cryoglobulins are Igs in the serum that precipitate in vitro at temperatures below
: • Clinical triad ... • Autoimmune diseases ... Types: • Type ... Labs/Diagnosis: ... Cryoglobulins #diagnosis