17 results
signs symptoms differential management pediatrics algorithm treatment causes comparison genetics hashimotos hashitoxicosis hyperthyroid hypothyroidism 21hydroxylasedeficiency 21ohd acromegaly adrenal ammonia bulimianervosa
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 ... #genetics #pathophysiology ... #peds #pediatrics
Infographic depicting the main pearls of various types of congenital adrenal hyperplasia for the medical student.
CongenitalAdrenalHyperplasia #diagnosis ... comparison #treatment #Peds ... #Endocrinology ... #Adrenal #pathophysiology
Hypothyroidism and Hyperthyroidism - Symptoms and Signs Hypothyroidism: - General - From asymptomatic to myxedema coma, “Like
- Gu: • Infertility ... MSc @AmyChung #Hypothyroid ... #Hyperthyroid # ... Symptoms #Signs #Diagnosis ... #endocrinology
Diabetes Insipidus vs Syndrome of Inappropriate ADH (SIADH) - Comparison Table Diabetes Insipidus - Inadequate ADH SIADH -
Diabetes Insipidus vs Syndrome ... Comparison #Table #Pathophysiology ... Signs #Symptoms #Diagnosis ... #Endocrinology
Tetralogy of Fallot Summary • Anatomy • Incidence • Pathophysiology • Presentation • Common Variants •
• Incidence • Pathophysiology ... Associated Genetic Syndromes ... Tetralogy #Fallot #diagnosis ... management #cardiology #peds
Weight Gain / Obesity - Differential Diagnosis Algorithm Decreased Expenditure: • Sedentary Lifestyle • Smoking Cessation
- Differential Diagnosis ... Polycystic Ovarian Syndrome ... • Hypothyroid ... • Cushing's Syndrome ... #Algorithm #endocrinology
Hypothyroidism – symptoms and signs. Symptoms: Tiredness/malaise, Weight gain, Anorexia, Cold intolerance, Poor memory, Change in appearance, Depression, Poor libido,
Carpal timel syndrome ... reflexes, Anaemia #Hypothyroid ... Signs #Symptoms #Diagnosis ... #PhysicalExam #Endocrinology
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 ... #peds #pediatrics
Algorithmic Approach to Hypothyroidism - Differential Diagnosis and Management Framework Central Hypothyroidism (Secondary or tertiary) ↓TSH, ↓FT4
- Differential Diagnosis ... Euthyroid sick syndrome ... #Differential #Diagnosis ... #algorithm #endocrinology ... #hypothyroid #Management
Laboratory Evaluation of Patients for Thyroid Disease Hyperthyroidism: • Graves disease - TSH low; free T4
Euthyroid sick syndrome ... disease course #hypothyroid ... #hyperthyroid # ... differential #diagnosis ... #endocrinology
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