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pathophysiology pediatrics peds 21hydroxylasedeficiency 21ohd acromegaly diabeticketoacidosis diagnosis dka glftap macroadenoma management masseffects mnemonic pituitary praderwilli sideeffects syndrome treatment
Prader-Willi Syndrome: Pathogenesis and clinical findings • Maternal uniparental disomy: inheriting 2 copies of maternal chromosome
Pathogenesis and clinical ... • Deletion of critical ... Syndrome Signs/Symptoms ... Obesity -> Type 2 diabetes ... PraderWilli #Syndrome #genetics
Pituitary Mass Effects - Pathogenesis and Clinical Findings • Pituitary turnors are almost always a benign
Pathogenesis and Clinical ... following order; GH, LH ... Signs / Symptoms ... Hyperprolactinemia • Diabetes ... #SideEffects #endocrinology
Diabetic Ketoacidosis (DKA) - Pathogenesis and Clinical Findings • Note: in DKA, body K+ is lost
Diabetic Ketoacidosis ... Pathogenesis and Clinical ... Signs/Symptoms/Complications ... pathophysiology #endocrinology ... #diabetes
21-Hydroxylase Deficiency (21-OHD): Pathogenesis and Clinical Findings Autosomal recessive mutation in CYP21A2 coding for the enzyme 21-OHase
Pathogenesis and Clinical ... Signs/Symptoms/Complications ... pathophysiology #genetics ... #endocrinology
Acromegaly - Diagnosis and Management Summary - GrepMed Handbook Clinical Presentation: • Classic Acromegaly: frontal
GrepMed Handbook Clinical ... phenytoin, minoxidil), genetic ... adenoma, ↓(TFT, LH ... Diagnosis #Management #Endocrinology
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