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diagnosis pediatrics peds signs symptoms comparison criteria deltawave diabetes differential ecgeducator ekg genetics management medstudent shortpr treatment wolffparkinsonwhite wpw 21hydroxylasedeficiency
Diabetes Insipidus vs Syndrome of Inappropriate ADH (SIADH) - Comparison Table Diabetes Insipidus - Inadequate ADH SIADH -
Diabetes Insipidus vs Syndrome ... Comparison #Table #Pathophysiology ... Symptoms #Diagnosis #Endocrinology
Kounis Syndrome (Allergic Angina) - Pathophysiology #Kounis #Syndrome #Allergic #Angina #Pathophysiology #cardiology
Kounis Syndrome ... Allergic Angina) - Pathophysiology ... #Kounis #Syndrome ... Allergic #Angina #Pathophysiology ... #cardiology
Prader-Willi Syndrome: Pathogenesis and clinical findings • Maternal uniparental disomy: inheriting 2 copies of maternal chromosome
Prader-Willi Syndrome ... =>Prader-Willi Syndrome ... delayed puberty -> Infertility ... #PraderWilli #Syndrome ... #genetics #pathophysiology
Wolfram syndrome (WS) is a form of monogenic diabetes that typically presents with diabetes mellitus in
Wolfram syndrome ... hypogonadism, infertility ... WOLFRAMSYNDROME #SUMMARY #ENDOCRINOLOGY
Wolff–Parkinson–White syndrome (WPW) Study Card #Pathophysiology #Diagnosis #Cardiology #MedStudent #EKG #WPW #WolffParkinsonWhite #DeltaWave #ShortPR #Criteria #ECGEducator
Wolff–Parkinson–White syndrome ... WPW) Study Card #Pathophysiology ... #Diagnosis #Cardiology
Pathophysiology of Diabetic Ketoacidosis (DKA) and Hyperglycemic Hyperosmolar Syndrome (HHS) Absolute Insulin deficit: - Type I DM:
Pathophysiology ... Hyperglycemic Hyperosmolar Syndrome ... #dka #hhs #pathophysiology ... #comparison #endocrinology
Tetralogy of Fallot Summary • Anatomy • Incidence • Pathophysiology • Presentation • Common Variants •
• Incidence • Pathophysiology ... Associated Genetic Syndromes ... diagnosis #management #cardiology
Wolff–Parkinson–White syndrome (WPW) is one of several disorders of the electrical system of the heart that
Wolff–Parkinson–White syndrome ... pre-excitation syndromes ... #Pathophysiology ... #Diagnosis #Cardiology
21-Hydroxylase Deficiency (21-OHD): Pathogenesis and Clinical Findings Autosomal recessive mutation in CYP21A2 coding for the enzyme 21-OHase
Hirsutism & acne • Infertility ... #21HydroxylaseDeficiency #21OHD #pathophysiology ... #genetics #endocrinology
Growth Hormone Excess - Pathogenesis and clinical findings • Acromegaly and gigantism share the same pathophysiology
share the same pathophysiology ... Carpal Tunnel Syndrome ... signs #symptoms #endocrinology ... #pathophysiology
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