12 results
pediatrics diagnosis differential causes genetics infant management neurology pathophysiology physicalexam 21hydroxylasedeficiency 21ohd brudzinskis dehydration disease disorders endocrinology evaluation floppy head
Causes of Pediatric Constipation - Differential Diagnosis Algorithm Dietary / Functional: • Insufficient Volume / Bulk Neurologic: •
Causes of Pediatric ... Constipation - ... Disease • Spinal Cord ... #Causes #Peds # ... Pediatrics
Pediatric Constipation - Differential Diagnosis Algorithm Dietary/Functional • lnsufficient Volume / Bulk Neurologic • Hirschsprung's Disease • Imperforate
Pediatric Constipation ... Differential Diagnosis Algorithm ... Disease • Spinal Cord ... #Diagnosis #Algorithm ... #Causes #Peds
Clinical features of shock from dehydration in an infant Decreased level of consciousness Sunken fontanelle Dry mucous
Clinical features ... in an infant Decreased ... #PhysicalExam #Signs ... #Dehydration #Peds ... #Pediatrics
Causes of Hypotonic Infant (Floppy Newborn) - Differential Diagnosis Algorithm Central Nervous System - Decreased LOC, Axial
Differential Diagnosis Algorithm ... Nervous System - Decreased ... • Central Core ... #Causes #Peds # ... Pediatrics
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 ... 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 ... #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
Multiple Sclerosis - Summary Multiple Sclerosis (MS) is an autoimmune-mediated neurodegenerative disease of the central nervous system
cognitive impairment, decreased ... Dysphagia • GI: Constipation ... patients with clinically ... stimulation Clinical ... Progressive MS (Spinal cord
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 ... endocrinology #peds ... #pediatrics
Evaluation of suspected incomplete Kawasaki Disease 1. AHA consensus recommendations 2. Infants ≤6 months old on day ≥7
if they have no clinical ... lack of tapering, decreased ... and lab signs ( ... #Diagnosis #Peds ... #Pediatrics #Kawasaki
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