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diagnosis peds congenital infections torch 21hydroxylasedeficiency 21ohd adrenal algorithm cah causes childhood congenitaladrenalhyperplasia diabetes functional genetics hematology hyperparathyroidism immunization incontinence
Diabetes Insipidus vs Syndrome of Inappropriate ADH (SIADH) - Comparison Table Diabetes Insipidus - Inadequate ADH SIADH -
ADH (SIADH) - Comparison ... Table Diabetes ... #Table #Pathophysiology ... #Signs #Symptoms ... #Diagnosis #Endocrinology
Infographic depicting the main pearls of various types of congenital adrenal hyperplasia for the medical student.
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 #Infections #Comparison ... #Table #pediatrics ... #diagnosis #symptoms
Congenital Infections - Comparison Table: Infections: Toxoplasma, Rubella, CMV, Treponema, Parvovirus B19, VZV, Herpes, Enterovirus Manifestations: Anemia, Bony
Congenital Infections - Comparison ... Table: Infections ... Congenital #Infections #Comparison ... #Table #pediatrics ... #diagnosis #symptoms
Types of Chronic Urinary Incontinence Type, Prevalence, Pathophysiology and Symptoms: - Stress - Urge - Mixed -
Type, Prevalence, Pathophysiology ... and Symptoms: ... Incontinence #Types #Comparison ... #Table #Stress
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 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
TRALI vs TACO - Transfusion Reactions TRALI: • Epidemiology: 0.1% of transfused patientsl • Risk factors: Critical
blood donor • Pathophysiology ... ARDS to explain symptoms ... transfusion • Pathophysiology ... hematology #diagnosis #comparison ... #table
21-Hydroxylase Deficiency (21-OHD): Pathogenesis and Clinical Findings Autosomal recessive mutation in CYP21A2 coding for the enzyme 21-OHase
Signs/Symptoms/Complications ... #21HydroxylaseDeficiency #21OHD #pathophysiology ... #genetics #endocrinology ... #peds #pediatrics
Childhood Immunization Schedule: Why we immunize • Diphtheria Toxin -> URT inflammation causes pseudomembrane with hardened
asymmetric reduction in tone ... hemorrhagic rash; symptoms ... non-specific viral symptoms ... Immunization #peds #pediatrics ... #pathophysiology
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