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differential causes peds treatment dementia genetics geriatrics management signs symptoms 21hydroxylasedeficiency 21ohd acromegaly acute adrenal adrenalmass aki alzheimersdisease antiphospholipid apls
Infographic depicting the main pearls of various types of congenital adrenal hyperplasia for the medical student.
#CAH #algorithm ... #causes #pediatrics ... CongenitalAdrenalHyperplasia #diagnosis ... treatment #Peds #Endocrinology ... #Adrenal #pathophysiology
Prader-Willi Syndrome: Pathogenesis and clinical findings • Maternal uniparental disomy: inheriting 2 copies of maternal chromosome
Prader-Willi Syndrome ... Pathogenesis and clinical ... delayed puberty -> Infertility ... #genetics #pathophysiology ... #peds #pediatrics
Gynecomastia - Differential Diagnosis a nd Workup Algorithm Gynecomastia is common in clinical practice, affecting ~50% of males
- Differential Diagnosis ... a nd Workup Algorithm ... Gynecomastia is common in clinical ... #Workup #Algorithm ... #endocrinology
Proposed Algorithm for Diagnosing Sarcoidosis Highly suggestive Clinicoradiological Findings → Clinical diagnosis (without biopsy) e.g. Löfgren's syndrome Suggestive
Proposed Algorithm ... Clinicoradiological Findings → Clinical ... Löfgren's syndrome ... #Sarcoidosis #Algorithm ... #diagnosis #Workup
Hypocalcemia - Differential Diagnosis Algorithm - Low and High PTH LOW PTH - Hypoparathyroid - Congenital (Pediatric)
- Differential Diagnosis ... Algorithm - Low ... - Congenital (Pediatric ... Tumor lysis syndrome ... #endocrinology
Short Stature - Differential Diagnosis Algorithm Normal Variant, Normal Puberty Onset (BA = CA) • Familial Short
- Differential Diagnosis ... Algorithm Normal ... #Differential #Diagnosis ... #Algorithm #endocrinology ... #causes #pediatrics
Major neurocognitive disorders (MNCD): Diagnosis and workup 1) Clinical diagnosis Cognitive impairment + loss of autonomy 2)
and workup ... 1) Clinical diagnosis ... Aphaso-apraxo-agnosia syndrome ... #Diagnosis #Geriatrics ... #Workup
21-Hydroxylase Deficiency (21-OHD): Pathogenesis and Clinical Findings Autosomal recessive mutation in CYP21A2 coding for the enzyme 21-OHase
Pathogenesis and Clinical ... Hirsutism & acne • Infertility ... #21HydroxylaseDeficiency #21OHD #pathophysiology ... #genetics #endocrinology ... #peds #pediatrics
Hyperglycemia - Differential Diagnosis Algorithm Diabetes Mellitus: • Impaired Glucose Tolerance • Type I Diabetes • Type
- Differential Diagnosis ... Algorithm Diabetes ... • Cushing's Syndrome ... agonists • Others Critical ... #Algorithm #endocrinology
Acute Kidney Injury - AKI Workup Algorithm and Differential Diagnosis Baseline Investigations: full blood count with differential,
Kidney Injury - AKI Workup ... Algorithm and Differential ... Diagnosis Baseline ... investigations depending on clinical ... #Injury #AKI #Workup
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