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cardiology 21hydroxylasedeficiency 21ohd algorithm alkaptonuria alzheimers anomalous antenatal aortic aorticvalve bicuspid blackurine complications cor cortriatriatum counseling decisionaid diabetes diabetic disease
Clinical Algorithm for Emergency Department Evaluation and Management of UTI in Febrile Infants and Young Children Urinary
Clinical Algorithm ... Evaluation and Management ... UTI #Algorithm #Diagnosis ... #Management #Febrile ... #Infant #Peds #
gestational diabetes algorithm #Infant #Diabetic #Mother #Pediatrics #Neonatology #IDM #NICU #OBGYN #Diagnosis #Pathophysiology #Maternal #Complications #Peds #Newborn
diabetes algorithm #Infant ... Diabetic #Mother #Pediatrics ... #NICU #OBGYN #Diagnosis ... #Pathophysiology ... Complications #Peds
Tetralogy of Fallot Summary • Anatomy • Incidence • Pathophysiology • Presentation • Common Variants •
Tetralogy of Fallot Summary ... • Incidence • Pathophysiology ... Tetralogy #Fallot #diagnosis ... #management #cardiology ... #peds #pediatrics
Alzheimer's Disease - Summary • Epidemiology • Pathophysiology • Risk Factors • Presentation • Diagnosis •
Alzheimer's Disease - Summary ... Epidemiology • Pathophysiology ... Treatment • Clinical ... #diagnosis #management ... #geriatrics
Cor triatriatum • Epidemiology • Etiology • Associated Lesions • Differentials Diagnosis • Anatomy - Sinister,
Physiology • Clinical ... Post-Operative Management ... #management #cardiology ... #summary #peds ... #pediatrics
Total Anomalous Pulmonary Venous Return (TAPVR) • Introduction • Classification • Pathophysiology of TAPVR • Presentation
Classification • Pathophysiology ... PVO Present • Diagnosis ... Return #TAPVR #diagnosis ... #peds #pediatrics ... #summary
Aortic Stenosis & Bicuspid Aortic Valve (AS) • Introduction & Pathophysiology • Classifications • Epidemiology •
Introduction & Pathophysiology ... Epidemiology • Clinical ... • Radiologic/Diagnostic ... AorticValve #cardiology #peds ... #pediatrics
21-Hydroxylase Deficiency (21-OHD): Pathogenesis and Clinical Findings Autosomal recessive mutation in CYP21A2 coding for the enzyme 21-OHase
Pathogenesis and Clinical ... deficiencies present in infants ... Hirsutism & acne • Infertility ... endocrinology #peds ... #pediatrics
Alkaptonuria (Black Urine Disease) Urine turns dark when left standing due to oxidation of homogentisic acid Clinical
homogentisic acid Clinical ... intervertebral discs Management ... Alkaptonuria #BlackUrine #Peds ... #Pediatrics #Diagnosis ... #Pathophysiology
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