10 results
diagnosis pediatrics peds symptoms dementia genetics 21hydroxylasedeficiency 21ohd alzheimersdisease anomalous arthritis attentiondeficithyperactivedisorder behavioraldisorder brocas brudzinskis cardiology classification clinical criteria differential
Alzheimer’s Disease: Pathogenesis and Clinical Findings Risk factor for Late Onset Alzheimer's (99% of cases): - Increasing
Complications: • Deficit ... semantic memory • Aphasia ... AlzheimersDisease #Dementia ... #pathophysiology ... #geriatrics #diagnosis
Aphasia - Pathophysiology and Clinical Findings Broca's Aphasia - Expressive language impairment: non-Fluent - Sensory speech areas
Aphasia - Pathophysiology ... Findings Broca's Aphasia ... Contralateral sensory deficits ... #Aphasia #Pathophysiology ... #diagnosis #signs
Major neurocognitive disorders (MNCD): Diagnosis and workup 1) Clinical diagnosis Cognitive impairment + loss of autonomy 2)
functions - Aphaso-apraxo-agnosia ... atrophy Lewy body dementia ... (parkinsonian signs ... Frontotemporal dementia ... Workup #Diagnosis #Geriatrics
Brudzinski’s Sign in Meningitis (first described in 19th century by Dr. Josef Brudzinski) Brudzinski's sign is characterized
Brudzinski’s Sign ... Brudzinski's sign ... While the pathophysiology ... of Brudzinski's sign ... #PhysicalExam #Pediatrics
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 Attention Deficit Hyperactive Disorder (ADHD): Pathogenesis and clinical findings - For diagnosis, must have either 26
Attention Deficit ... Hyperactive Disorder (ADHD ... with inattentive ADHD ... BehavioralDisorder #Pathophysiology ... diagnosis #symptoms #signs
Total Anomalous Pulmonary Venous Return (TAPVR) • Introduction • Classification • Pathophysiology of TAPVR • Presentation
Classification • Pathophysiology ... Classic “snowman sign ... cardiology #peds #pediatrics
Prader-Willi Syndrome: Pathogenesis and clinical findings • Maternal uniparental disomy: inheriting 2 copies of maternal chromosome
Prader-Willi Syndrome Signs ... Syndrome #genetics #pathophysiology ... #peds #pediatrics
Acute Otitis Media: Pathogenesis and Clinical Findings (in Children) Upper Respiratory Tract Infection: - Bacterial: Streptococcus
#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
Joint Approach to Juvenile Idiopathic Arthritis (JIA) JIA is a clinical diagnosis - Diagnostic criteria: • One
symmetry • Look for signs ... Methotrexate • 2nd line: Add ... Arthritis #JIA #pediatrics
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