23 results
diagnosis neurology differential signs symptoms treatment nephrology urology cns guillain hyponatremia peds physicalexam syndrome 21hydroxylasedeficiency 21ohd acidosis algorithm als amyotrophic
Causes of Pediatric Constipation - Differential Diagnosis Algorithm Dietary / Functional: • Insufficient Volume / Bulk Neurologic: •
Causes of Pediatric ... Volume / Bulk Neurologic ... Pseudo-obstruction Neurologic ... Congenita • Guillain-Barré ... Syndrome • Muscular Dystrophy
Gowers' Sign on Physical Exam Caused by proximal muscle weakness typically seen in muscular dystrophy #Gowers #Sign #PhysicalExam
Gowers' Sign on ... Physical Exam Caused ... #Gowers #Sign ... #PhysicalExam #neurology ... clinical #video #pediatrics
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 Distal Renal Tubular Acidosis (RTA) Type 1 Totally scuppers the kidney's acidification mechanism. Will be
diagnosis with direct urine ... Failure to acidify urine ... pH <5.5 - Dr ... Distal #Diagnosis #Management ... #Nephrology #Causes
Guillain-Barre Syndrome - Summary Acute AIDP that presents with rapidly progressive flaccid weakness Epidemiology: • 1-2 cases/100,000 per
Epidemiology: • 1-2 cases ... Pathophysiology ... feet • Pain: Due ... Syndrome #diagnosis #management ... #treatment #neurology
Management of Pediatric Kidney Stones Acute Managment: • Pain relief: NSAIDs, opioids • Facilitating passage of stone:
Management of Pediatric ... Kidney Stones Acute Managment ... retrieve stone using urine ... ascorbic acid Dr ... #Pediatrics #nephrology
Guillain-Barré Syndrome (GBS) Acute autoimmune demyelinating polyradiculoneuropathy that presents with rapidly progressive flaccid weakness Epidemiology: • Incidence: 1
Guillain-Barré Syndrome ... Incidence: 1 to 2 cases ... the underlying pathophysiology ... Syndrome #diagnosis #management ... #neurology
Causes of Secondary Hypertension - Workup and Differential Diagnosis Approach (when evaluation should be done): 1. Severe or
heart failure, neurologic ... renal bruit or signs ... Neurologic disorders ... , and Guillain-Barre ... Syndrome - Dr
21-Hydroxylase Deficiency (21-OHD): Pathogenesis and Clinical Findings Autosomal recessive mutation in CYP21A2 coding for the enzyme 21-OHase
enzyme 21-OHase causes ... Signs/Symptoms/Complications ... non-arousable, decr urine ... #21HydroxylaseDeficiency #21OHD #pathophysiology ... endocrinology #peds #pediatrics
SIADH Treatment Options 1. Treat underlying cause of SIADH: Pain, Primary lung pathology, Post-operative phenomenon, Medications, Basically
0.9% NS • If Urine ... boluses at a time • Re-check ... Hypotension, Increased urine ... SatyaPatelMD #SIADH #Management ... #hyponatremia #nephrology
Intracranial Hemorrhage (ICH) and Increased Intracranial Pressure (ICP) - Pathophysiology ICH Management: 1. Manage Blood Pressure •
Pressure (ICP) - Pathophysiology ... ICH Management ... = dilated BV = raises ... #neurology #neurosurgery ... #management
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