40 results
Infographic depicting the main pearls of various types of congenital adrenal hyperplasia for the medical student.
CAH #algorithm #causes ... CongenitalAdrenalHyperplasia #diagnosis ... treatment #Peds #Endocrinology ... #Adrenal #pathophysiology
Causes of B12 deficiency. 

This great diagram shows normal absorption and outlines most possible causes. At
Causes of B12 deficiency ... most possible causes ... the top is a B12-deficient ... #Differential #Causes ... #Diagnosis #Pathophysiology
Amenorrhea - Differential Diagnosis Algorithm
Elevated FSH
 • Premature Ovarian Failure
 • Menopa use
 • Spontaneous
Bleed With
- Differential Diagnosis ... Congenital GnRH Deficiency ... #Differential #Diagnosis ... #Algorithm #endocrinology ... #causes
Hypophosphatemia - Differential Diagnosis Algorithm

Transcellular Shift
 • Recovery From DKA
 • Refeeding Syndrome
 • Acute Respiratory
- Differential Diagnosis ... • Vitamin D Deficiency ... #Differential #Diagnosis ... #Algorithm #endocrinology ... #causes
Iron Deficiency in Heart Failure
Pathophysiology:
Chronic heart failure leads to an increase in inflammatory cytokines → Inflammation
Iron Deficiency ... Heart Failure Pathophysiology ... → Inflammation causes ... and iron release Diagnosis ... endpoint of all-cause
Hyperphosphatemia - Differential Diagnosis Algorithm
Transcellular Shift:
 • Rhabdomyolysis
 • Tumor Lysis
 • Metabolic or Respiratory Acidosis
- Differential Diagnosis ... Acidosis • Insulin Deficiency ... #Differential #Diagnosis ... #Algorithm #endocrinology ... #causes
Primary Adrenal Insufficiency
Addison's Disease - Damage of the adrenal glands with lack of cortisol, androgens and
aldosterone Causes ... : Most Common Causes ... Serum DHEAS Diagnosis ... addisons #disease #endocrinology ... #diagnosis #signs
Short Stature - Differential Diagnosis Algorithm
Normal Variant, Normal Puberty Onset (BA = CA)
 • Familial Short
- Differential Diagnosis ... Disease • GH Deficiency ... • IGF-I Deficiency ... #Algorithm #endocrinology ... #causes #pediatrics
21-Hydroxylase Deficiency (21-OHD): Pathogenesis and Clinical Findings
Autosomal recessive mutation in CYP21A2 coding for the enzyme 21-OHase
21-Hydroxylase Deficiency ... enzyme 21-OHase causes ... amount of enzyme deficiency ... #21HydroxylaseDeficiency #21OHD #pathophysiology ... #genetics #endocrinology
Ketosis Disorders
Ketone bodies are a normal metabolic energy source. Excessive unregulated production of ketones, often accompanied
ketoacidosis (DKA) - caused ... complete insulin deficiency ... Glucosuria causes ... #differential #diagnosis ... #management #endocrinology