18 results
Congenital TORCH Infections

Dr. Natalie Marshall @MicrobeNat

#Congenital #Infections #Comparison #Table #pediatrics #diagnosis #symptoms #TORCH
Congenital TORCH ... @MicrobeNat #Congenital ... Comparison #Table #pediatrics ... #diagnosis #symptoms
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 ... Endocrinology #Adrenal #pathophysiology
Congenital Infections - Comparison Table:
Infections: Toxoplasma, Rubella, CMV, Treponema, Parvovirus B19, VZV, Herpes, Enterovirus
Manifestations: Anemia, Bony
Congenital Infections ... Thrombocytopenia #Congenital ... Comparison #Table #pediatrics ... #diagnosis #symptoms
Hypokalemia Evaluation Algorithm

Before evaluating hypokalemia, life threatening complications such as arrhythmias and paralysis should be looked
treated with IV potassium ... Liddle's syndrome, Congenital ... Non-reabsorbable anions ... #Hypokalemia #diagnosis ... #differential #potassium
Thyrotoxic Periodic Paralysis - Illness Script
 • Epidemiology: Asian men age 20-30 with hyperthyroidism of any
and menses • Pathophysiology ... thyroid hormone • Symptoms ... • Treatment: Potassium ... hyperthyroidism, Potassium ... Periodic #Paralysis #diagnosis
Pediatric Parasomnias and Nightmares: Pathogenesis and clinical findings

Parasomnias - Micro-arousal episodes during SWS ->
Intense activation of
Pediatric Parasomnias ... Parasomnias #Nightmares #Pediatrics ... #Peds #pathophysiology ... #symptoms #pharmacology ... #diagnosis
Primary Adrenal Insufficiency
Addison's Disease - Damage of the adrenal glands with lack of cortisol, androgens and
sodium • ↑ Serum potassium ... Serum DHEAS Diagnosis ... Check sodium, potassium ... insufficiency #addisons ... endocrinology #diagnosis
Alzheimer’s Disease: Pathogenesis and Clinical Findings
Risk factor for Late Onset Alzheimer's (99% of cases):
 - Increasing
chromosome 21) Signs / Symptoms ... AlzheimersDisease #Dementia #pathophysiology ... #geriatrics #diagnosis ... #signs #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 ... #21HydroxylaseDeficiency #21OHD #pathophysiology ... endocrinology #peds #pediatrics
Central Retinal Artery Occlusion: Pathogenesis and clinical findings
 • Inflammatory Disease: (i.e. GCA, SLE, GPA) ->
, arrhythmias, congenital ... Ganglion cells and axons ... Occlusion #CRAO #pathophysiology ... ophthalmology #diagnosis ... #signs #symptoms