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pediatrics 21hydroxylasedeficiency 21ohd brudzinskis endocrinology growthplate humeralhead meningitis physicalexam pocus praderwilli shoulder sign syndrome ultrasound video
Prader-Willi Syndrome: Pathogenesis and clinical findings • Maternal uniparental disomy: inheriting 2 copies of maternal chromosome
Pathogenesis and clinical ... • Deletion of critical ... PraderWilli #Syndrome #genetics ... #pathophysiology ... #peds #pediatrics
21-Hydroxylase Deficiency (21-OHD): Pathogenesis and Clinical Findings Autosomal recessive mutation in CYP21A2 coding for the enzyme 21-OHase
Pathogenesis and Clinical ... , vomiting • Late ... #21HydroxylaseDeficiency #21OHD #pathophysiology ... #genetics #endocrinology ... #peds #pediatrics
Brudzinski’s Sign in Meningitis (first described in 19th century by Dr. Josef Brudzinski) Brudzinski's sign is characterized
While the pathophysiology ... meningitis, it has low sensitivity ... Sign #Meningitis #Clinical ... #PhysicalExam #Pediatrics ... #Peds
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 Humeral Head Growth Plate on Shoulder POCUS A 15yo male presents with shoulder pain. Which of the
Humeral Head Growth Plate ... There is a growth plate ... Shoulder #POCUS #MSK ... #Peds #Pediatrics ... #clinical #ultrasound
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