11 results
diagnosis management endocrinology heartfailure algorithm cardiomyopathy 21hydroxylasedeficiency 21ohd adrenal age cah comparison congenitaladrenalhyperplasia congestive deficiency dilated encephalopathy fallot hfpef high
Congestive Heart Failure - Causes, Pathophysiology and Differential Diagnosis • Dilated Cardiomyopathy • Hypertrophic Cardiomyopathy
, Pathophysiology ... Infiltrative • Genetic ... Diagnosis #cardiology ... #HFrEF #HFpEF # ... CHF
Infographic depicting the main pearls of various types of congenital adrenal hyperplasia for the medical student.
various types of congenital ... CAH #algorithm #causes ... diagnosis #comparison #treatment ... #Peds #Endocrinology ... #Adrenal #pathophysiology
Etiologies of dilated cardiomyopathy. HF, heart failure; HFrEF, heart failure with reduced ejection fraction; HIV, human
; HFrEF, heart failure ... - Genetic ... cardiomyopathy #differential ... #diagnosis #cardiology ... #causes
Tetralogy of Fallot Summary • Anatomy • Incidence • Pathophysiology • Presentation • Common Variants •
• Incidence • Pathophysiology ... • Associated Genetic ... diagnosis #management #cardiology ... #peds #pediatrics ... #treatment
High Output Heart Failure - Pathophysiology and Differential Diagnosis Obesity - Systemic Vasodilation, Vasoactive Adipokines Arteriovenous Fistula -
and Differential ... Arteriovenous Fistula - Congenital ... #HeartFailure #CHF ... Diagnosis #cardiology ... #causes
Iron Deficiency in Heart Failure Pathophysiology: Chronic heart failure leads to an increase in inflammatory cytokines → Inflammation
Heart Failure Pathophysiology ... functional ID) Treatment ... iron #deficiency #CHF ... #HFrEF #heartfailure ... diagnosis #management #cardiology
Short Stature - Differential Diagnosis Algorithm Normal Variant, Normal Puberty Onset (BA = CA) • Familial Short
Hypothyroidism • Congenital ... Panhypopituitarism Treatment ... Cystic Fibrosis, CHF ... endocrinology #causes ... #pediatrics
21-Hydroxylase Deficiency (21-OHD): Pathogenesis and Clinical Findings Autosomal recessive mutation in CYP21A2 coding for the enzyme 21-OHase
enzyme 21-OHase causes ... also known as "congenital ... #21HydroxylaseDeficiency #21OHD #pathophysiology ... #genetics #endocrinology ... #peds #pediatrics
Age Distribution of Hypertension Etiologies < 1 month - Renal arterial thrombosis - Congenital renal disease -
thrombosis - Congenital ... - Mendelian genetic ... #Hypertension #Causes ... #age #pediatrics ... #peds
Posterior Reversible Encephalopathy Syndrome (PRES) Overview Clinico-Radiological Syndrome, characterized by: • Headache • Seizures • Altered mental
Etiology: • Pathophysiology ... Reversible course Differential ... the underlying cause ... • Treatment of ... until cause identified
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