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diagnosis pediatrics differential management neurology shock causes criticalcare genetics overview physicalexam 21hydroxylasedeficiency 21ohd als amyotrophic brudzinskis dehydration disease disorders endocrinology
Clinical features of shock from dehydration in an infant Decreased level of consciousness Sunken fontanelle Dry mucous
Clinical features ... in an infant Decreased ... urine output Cold ... #PhysicalExam #Signs ... #Dehydration #Peds
Prader-Willi Syndrome: Pathogenesis and clinical findings • Maternal uniparental disomy: inheriting 2 copies of maternal chromosome
Pathogenesis and clinical ... Prader-Willi Syndrome Signs ... , sleep apnea, cor ... Syndrome #genetics #pathophysiology ... #peds #pediatrics
Brudzinski’s Sign in Meningitis (first described in 19th century by Dr. Josef Brudzinski) Brudzinski's sign is characterized
Brudzinski’s Sign ... causes spinal cord ... While the pathophysiology ... #Meningitis #Clinical ... PhysicalExam #Pediatrics #Peds
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 Spinal Cord Disorders - Differential Diagnosis Framework Spinal cord neurological lesion: Clinical findings: • Symptoms and signs below
Spinal Cord Disorders ... neurological lesion: Clinical ... • Symptoms and signs ... Cauda equina- decreased ... differential #algorithm
Shock Overview A state of tissue hypoxia due to decreased or dysregulated oxygen delivery or extraction, resulting
death Common Clinical ... Ext: warm vs. cold ... anaphylaxis, toxins/meds ... EmmGeezee #Shock #Classification ... differential #causes #classification
Shock Overview A state of tissue hypoxia due to decreased or dysregulated oxygen delivery or extraction, resulting
death Common Clinical ... Ext: warm vs. cold ... anaphylaxis, toxins/meds ... EmmGeezee #Shock #Classification ... differential #causes #classification
Transverse Myelitis Overview Focal inflammatory disorder of the spinal cord resulting in rapid onset of weakness, sensory
of the spinal cord ... monophasic Pathophysiology ... Transverse Myelitis - Clinical ... - Reflexes: decreased ... • Bilateral signs
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 ... Late (shock): cold ... #21HydroxylaseDeficiency #21OHD #pathophysiology ... endocrinology #peds
Amyotrophic Lateral Sclerosis (ALS) Summary ALS: combination of the clinical examination finding of amyotrophy with the pathologic
combination of the clinical ... lateral sclerosis Pathophysiology ... cellular function Clinical ... multiple spinal cord ... - Fatigue and decreased
Evaluation of suspected incomplete Kawasaki Disease 1. AHA consensus recommendations 2. Infants ≤6 months old on day ≥7
if they have no clinical ... purposes of this algorithm ... lack of tapering, decreased ... and lab signs ( ... #Diagnosis #Peds
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