13 results
Ketosis Disorders - Comparison Table
 • Starvation Ketosis
 • Alcoholic Ketoacidosis (AKA)
 • Diabetic Ketoacidosis (DKA)
Ketosis Disorders - Comparison ... Ketoacidosis (DKA ... • Hyperglycemic ... diagnosis #management #endocrinology ... #comparison #table
Pathophysiology of Diabetic Ketoacidosis (DKA) and Hyperglycemic Hyperosmolar Syndrome (HHS)
Absolute Insulin deficit:
 - Type I DM:
Pathophysiology ... Ketoacidosis (DKA ... ) and Hyperglycemic ... Polydipsia #dka ... #comparison #endocrinology
DKA vs HHS
 - Think of DKA and HHS on a spectrum of hyperglycemic emergencies
 -
a spectrum of hyperglycemic ... #HHS #comparison ... laboratory #diagnosis #endocrinology ... #comparison #diabetic ... #hyperosmolar #hyperglycemic
Infographic depicting the main pearls of various types of congenital adrenal hyperplasia for the medical student.
various types of congenital ... algorithm #causes #pediatrics ... CongenitalAdrenalHyperplasia #diagnosis #comparison ... treatment #Peds #Endocrinology ... #Adrenal #pathophysiology
Congenital TORCH Infections

Dr. Natalie Marshall @MicrobeNat

#Congenital #Infections #Comparison #Table #pediatrics #diagnosis #symptoms #TORCH
Congenital TORCH ... @MicrobeNat #Congenital ... #Infections #Comparison ... #Table #pediatrics ... #diagnosis #symptoms
Pathyophysiology - hyperglycemic crises in patients with diabetes 
Key signs/symptoms of HHS/DKA:
Both: Polyuria, polydipsia, weight loss,
Pathyophysiology ... - hyperglycemic ... diabetes Key signs/symptoms ... of HHS/DKA: Both ... , hypotension) DKA
Diabetes Insipidus vs Syndrome of Inappropriate ADH (SIADH) - Comparison Table

Diabetes Insipidus - Inadequate ADH
SIADH -
ADH (SIADH) - Comparison ... Insipidus #SIADH #Comparison ... #Table #Pathophysiology ... #Signs #Symptoms ... #Diagnosis #Endocrinology
Congenital Infections - Comparison Table:
Infections: Toxoplasma, Rubella, CMV, Treponema, Parvovirus B19, VZV, Herpes, Enterovirus
Manifestations: Anemia, Bony
Congenital Infections ... - Comparison Table ... #Infections #Comparison ... #Table #pediatrics ... #diagnosis #symptoms
21-Hydroxylase Deficiency (21-OHD): Pathogenesis and Clinical Findings
Autosomal recessive mutation in CYP21A2 coding for the enzyme 21-OHase
also known as "congenital ... Signs/Symptoms/Complications ... Hyperkalemia, Hypoglycemia ... #genetics #endocrinology ... #peds #pediatrics
Hyperparathyroidism - Primary vs Secondary vs Tertiary 
Lab Comparison:
 • Primary Hyperparathyroidism: ↑→PTH, ↑Calcium, ↑Vitamin D,
Tertiary Lab Comparison ... Phosphate Physical Symptoms ... pain Psychiatric Symptoms ... Hyperparathyroidism #diagnosis #endocrinology ... Secondary #Tertiary #pathophysiology