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diagnosis neurology differential nephrology algorithm treatment epilepticus hyponatremia status 2 21hydroxylasedeficiency 21ohd 3 acidosis als amyotrophic arteritis chagas child clinical
Causes of Pediatric Constipation - Differential Diagnosis Algorithm Dietary / Functional: • Insufficient Volume / Bulk Neurologic: •
Causes of Pediatric ... Volume / Bulk Neurologic ... Pseudo-obstruction Neurologic ... Syndrome • Muscular Dystrophy ... #Peds #Pediatrics
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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 Status Epilepticus - Management Seizure > 5 mins or two seizures without complete recovery between them PEDS Benzo Dose
Epilepticus - Management ... between them PEDS ... Intubation - Dr ... treatment #algorithm #peds ... #pediatrics #neurology
Urine Color - Differential Diagnosis Red Urine: • Medical conditions: bleeding, porphyria, factitious disorder • Meds: rifampin,
: • Any cause of ... Pseudomonas • Meds ... dyes typically cause ... : propofol - Dr ... discoloration #nephrology
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
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
THE LIMPING OR NON-WEIGHT BEARING CHILD PATHWAY RED FLAGS - In all cases there are specific markers which
FLAGS - In all cases ... there are specific ... splenomegaly, abnormal neurology ... Pathway #Child #Peds ... #Pediatrics #Diagnosis
Myasthenia Gravis Overview Myasthenia Gravis is an autoimmune disorder of the postsynaptic neuromuscular junction. Ab to
syndrome - Myotonic dystrophy ... test - Cogan sign ... - Peek sign ... Gravis #diagnosis #management ... #neurology
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 ... 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
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