56 results
signs symptoms neurology peds video management differential treatment dementia geriatrics ophthalmology endocrinology msk barre bilateral cardiology cirrhosis genetics guillain hepatology
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
Prune Belly (Eagle-Barrett) Syndrome - Abdominal Examination @MIRtirizado #Prune #Belly #Syndrome #Abdominal #PhysicalExam #clinical #video #pediatrics #Eagle #Barrett
Eagle-Barrett) Syndrome ... #Prune #Belly #Syndrome ... #Abdominal #PhysicalExam ... #clinical #video ... #pediatrics #Eagle
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 Tetralogy of Fallot Summary • Anatomy • Incidence • Pathophysiology • Presentation • Common Variants •
• Incidence • Pathophysiology ... Associated Genetic Syndromes ... Tetralogy #Fallot #diagnosis ... cardiology #peds #pediatrics
Pediatric Inflammatory Multisystem Syndrome Temporally associated with SARS-CoV-2 infection (PIMS-TS) Clinical features all: fever > 101.3 F most: oxygen
Pediatric Inflammatory ... Multisystem Syndrome ... infection (PIMS-TS) Clinical ... #Inflammatory #Syndrome ... #coronavirus #diagnosis
Alzheimer's Disease - Summary • Epidemiology • Pathophysiology • Risk Factors • Presentation • Diagnosis •
Epidemiology • Pathophysiology ... Presentation • Diagnosis ... Treatment • Clinical ... Disease #Summary #diagnosis ... #management #geriatrics
Aortic Stenosis & Bicuspid Aortic Valve (AS) • Introduction & Pathophysiology • Classifications • Epidemiology •
Introduction & Pathophysiology ... Epidemiology • Clinical ... • Radiologic/Diagnostic ... cardiology #peds #pediatrics
Purple Urine Bag Syndrome Chronic, indwelling catheter + bacteriuria (Providencia, Klebsiella, E.coli*) + alkaline urine Tryptophan → Indoxyl
Purple Urine Bag Syndrome ... Purple #Urine #Bag #Syndrome ... #PUBS #pathophysiology ... #clinical #photo ... #differential #diagnosis
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 ... endocrinology #peds #pediatrics
Erb's Palsy and Ptosis on Newborn Examination after Delivery Two issues here related to shoulder dystocia with
from Horner’s syndrome ... Ptosis #Newborn #physicalExam ... #pediatrics #obgyn ... #obstetrics #clinical
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 Patellofemoral Syndrome - Pathogenesis and clinical findings • Anterior Knee Pain with possible symptoms of 'catching'
Patellofemoral Syndrome ... Pathogenesis and clinical ... Patellofemoral #Syndrome ... #pathophysiology ... #diagnosis #signs
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