50 results
Causes of Apparent Life Threatening Event (ALTE) - Differential Diagnosis Algorithm
Cardiac:
 • Congenital Heart Disease
 •
Causes of Apparent ... Disturbances Neurologic ... Aspiration • Breath-holding ... Hernia Witnessed Choking ... Diagnosis #Algorithm #Causes
Bell's Palsy
Bell’s Palsy is a damage, acute weakness, or paralysis of the Facial nerve (7th CN),
an identifiable cause ... The cause is unknown ... #Bells #Palsy #neurology ... #anatomy #pathophysiology
Erythroderma - Diagnostic Algorithm. Pathophysiology: 1) Extensive cutaneous capillary dilation, results in widespread exfoliation of the
Pathophysiology: ... Causes: 1) Exfoliative ... Histamine 4) Skin-homing
Pseudobulbar Affect
Characteristics (These episodes usually cause distress and impairment in occupational or social functioning):
 - Extreme
episodes usually cause ... of laughter and crying ... Sclerosis (ALS) (*main cause ... Pseudobulbar #Affect #neurology
Gitelman Syndrome Pathophysiology
Gitelman Syndrome is a rare autosomal recessive salt-losing tubulopathy with a prevalence of 1-
Gitelman Syndrome Pathophysiology ... recessive salt-losing ... Gitelman #Syndrome #Pathophysiology ... #nephrology #diagnosis
Polyuria - Differential Diagnosis Algorithm
Urine Output > 3L /day
Water Diuresis (Urine Osm <100 mOsm/kg)
 • Primary
Water and solute loading ... Diagnosis #Algorithm #causes ... #nephrology
Causes of Hyponatremia - Differential Diagnosis Algorithm
Hypovolemia, UNa > 20: 
 • Renal losses, Diuretic excess,
Causes of Hyponatremia ... deficiency, Salt-losing ... Diagnosis #Algorithm #Causes ... #nephrology
NSAID vs ACEI/ARB effects on the Kidneys

Remember that NSAIDs and ACEI/ARB therapy have opposing effects on
NSAIDs cause vasoconstriction ... use shouldn't cause ... ACEIARB #Effects #Nephrology ... #Renal #Pathophysiology
Diabetes – diabetic nephropathy
Majority of the literature in the area is applied to the diabetic nephropathy
be the primary cause ... - Cytokines #Pathophysiology ... #Nephrology #CKD
21-Hydroxylase Deficiency (21-OHD): Pathogenesis and Clinical Findings
Autosomal recessive mutation in CYP21A2 coding for the enzyme 21-OHase
mutation in CYP21A2 coding ... enzyme 21-OHase causes ... #21HydroxylaseDeficiency #21OHD #pathophysiology