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diagnosis signs pediatrics peds genetics psychiatry 21hydroxylasedeficiency 21ohd adhd aphasia attentiondeficithyperactivedisorder behavioraldisorder bipolar brocas criteria dementia disorder endocrinology geriatrics meningitis
Brudzinski’s Sign in Meningitis (first described in 19th century by Dr. Josef Brudzinski) Brudzinski's sign is characterized
Brudzinski’s Sign ... Josef Brudzinski ... While the pathophysiology ... #Clinical #Video ... #PhysicalExam #Pediatrics
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 Alzheimer’s Disease: Pathogenesis and Clinical Findings Risk factor for Late Onset Alzheimer's (99% of cases): - Increasing
Pathogenesis and Clinical ... : • Deficit in ... aggression #AlzheimersDisease ... #Dementia #pathophysiology ... #signs #symptoms
Prader-Willi Syndrome: Pathogenesis and clinical findings • Maternal uniparental disomy: inheriting 2 copies of maternal chromosome
Pathogenesis and clinical ... Prader-Willi Syndrome Signs ... /Symptoms/Complications ... Syndrome #genetics #pathophysiology ... #peds #pediatrics
Aphasia - Pathophysiology and Clinical Findings Broca's Aphasia - Expressive language impairment: non-Fluent - Sensory speech areas
Aphasia - Pathophysiology ... and Clinical Findings ... Contralateral sensory deficits ... #diagnosis #signs ... #symptoms #Brocas
Bipolar Disorder: Pathogenesis and Clinical Findings • Disruption of emotional homeostasis • Oscillation between mood states
Pathogenesis and Clinical ... Euthymic Mood - Definite ... MoodDisorders #Diagnosis #Pathophysiology ... #Signs #Symptoms
Acute Otitis Media: Pathogenesis and Clinical Findings (in Children) Upper Respiratory Tract Infection: - Bacterial: Streptococcus
Pathogenesis and Clinical ... #OtitisMedia #pathophysiology ... #diagnosis #symptoms ... #signs #peds #pediatrics
Attention Deficit Hyperactive Disorder (ADHD): Pathogenesis and clinical findings - For diagnosis, must have either 26
Attention Deficit ... Pathogenesis and clinical ... have either 26 symptoms ... BehavioralDisorder #Pathophysiology ... #signs #psychiatry
21-Hydroxylase Deficiency (21-OHD): Pathogenesis and Clinical Findings Autosomal recessive mutation in CYP21A2 coding for the enzyme 21-OHase
Pathogenesis and Clinical ... Signs/Symptoms/Complications ... #21HydroxylaseDeficiency #21OHD #pathophysiology ... endocrinology #peds #pediatrics
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