15 results
diagnosis symptoms peds physicalexam cardiology clinical duchenne dystrophy genetics geriatrics gowers management muscular sign video 21hydroxylasedeficiency 21ohd agerelated aging alzheimersdisease
Atrioventricular Septal Defect aka AV canal defect aka endocardial cushion defect • Epidemiology and Associations • Embryology
Defect aka AV canal ... Physical Exam • Pathophysiology ... Outcomes by Cara ... Holton, MD @crholton ... management #peds #pediatrics
Gowers' Sign on Physical Exam Seen in this patient with Duchenne muscular dystrophy (DMD) #Gowers #Sign #PhysicalExam #neurology
Gowers' Sign on ... muscular dystrophy (DMD ... ) #Gowers #Sign ... #PhysicalExam #neurology ... clinical #video #pediatrics
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 Age Related Physiologic Changes and Anesthesia Implications - Mark Harris, MD MPH @ https://twitter.com/MarkHarrisMD #Geriatrics #Aging #Anesthesia
and Anesthesia Implications ... - Mark Harris, MD ... MarkHarrisMD #Geriatrics ... Aging #Anesthesia #Pathophysiology
Total Anomalous Pulmonary Venous Return (TAPVR) • Introduction • Classification • Pathophysiology of TAPVR • Presentation
Classification • Pathophysiology ... Classic “snowman sign ... Outcomes by Cara ... Holton, MD @crholton ... cardiology #peds #pediatrics
Prader-Willi Syndrome: Pathogenesis and clinical findings • Maternal uniparental disomy: inheriting 2 copies of maternal chromosome
Prader-Willi Syndrome Signs ... /Symptoms/Complications ... Syndrome #genetics #pathophysiology ... #peds #pediatrics
Alzheimer’s Disease: Pathogenesis and Clinical Findings Risk factor for Late Onset Alzheimer's (99% of cases): - Increasing
chromosome 21) Signs ... / Symptoms / Complications ... AlzheimersDisease #Dementia #pathophysiology ... #geriatrics #diagnosis ... #signs #symptoms
Acute Otitis Media: Pathogenesis and Clinical Findings (in Children) Upper Respiratory Tract Infection: - Bacterial: Streptococcus
resolve by 72 hours Complications ... #OtitisMedia #pathophysiology ... diagnosis #symptoms #signs ... #peds #pediatrics
21-Hydroxylase Deficiency (21-OHD): Pathogenesis and Clinical Findings Autosomal recessive mutation in CYP21A2 coding for the enzyme 21-OHase
Signs/Symptoms/Complications ... #21HydroxylaseDeficiency #21OHD #pathophysiology ... endocrinology #peds #pediatrics
Trendelenburg Gait: Pathogenesis and clinical findings Skeletal Pathology of the Hip • Arthritis • Congenital hip dysplasia
Chondrodysplasia Neurologic ... in the Spinal canal ... Trendelenburg #Gait #pathophysiology ... causes #symptoms #signs
Gowers' Sign on Physical Exam Indicative of proximal muscle weakness in muscular dystrophy. #Gowers #Sign #PhysicalExam #neurology #clinical
Gowers' Sign on ... #Gowers #Sign #PhysicalExam ... #neurology #clinical ... #video #pediatrics ... muscular #dystrophy #DMD
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