14 results
Brudzinski's Sign on Physical Exam - Meningitis

#Brudzinskis #Sign #PhysicalExam #clinical #video #neurology #peds #pediatrics #meningitis
Brudzinski's Sign ... #Brudzinskis ... #clinical #video ... #neurology #peds ... #pediatrics #meningitis
Brudzinski’s Sign in Meningitis (first described in 19th century by Dr. Josef Brudzinski)

Brudzinski's sign is characterized
Brudzinski’s Sign ... #Sign #Meningitis ... #Clinical #Video ... #PhysicalExam #Pediatrics ... #Peds
Brudzinski's Sign on Physical Exam - Meningitis

via  @TheIntern254

#Brudzinskis #Sign #PhysicalExam #clinical #video #neurology #peds #pediatrics
Brudzinski's Sign ... #Sign #PhysicalExam ... #clinical #video ... #neurology #peds ... #pediatrics #meningitis
Brudzinski's sign is a physically demonstrable symptom of meningitis. It is characterized by reflexive flexion of
Brudzinski's sign ... physically demonstrable symptom ... of meningitis. ... #Brudzinskis #sign ... #clinical #video
Practical Pediatric Viral Rash Algorithm

Child presenting with rash and current/ recent symptoms of viral illness but
Practical Pediatric ... five days and no signs ... / symptoms of sepsis ... or meningitis — ... #Peds #Diagnosis
Clinical features of shock from dehydration in an infant

Decreased level of consciousness 
Sunken fontanelle 
Dry mucous
Clinical features ... #PhysicalExam #Signs ... #Symptoms #Shock ... #Dehydration #Peds ... #Pediatrics
Kernig's Sign in Meningitis

Kernig's sign is present if the patient, in the supine position with the
Kernig's Sign in ... Meningitis Kernig's ... #Meningitis #Clinical ... #PhysicalExam #Pediatrics ... #Peds #neurology
Clinical Features and Complications of Measles

Rash:
Spreads downwards, from behind the ears to the whole Of the
Clinical Features ... Kopliks KoplikSpots #Peds ... #Pediatrics #Timeline ... #Signs #Symptoms
Prader-Willi Syndrome: Pathogenesis and clinical findings
 • Maternal uniparental disomy: inheriting 2 copies of maternal chromosome
Pathogenesis and clinical ... Prader-Willi Syndrome Signs ... /Symptoms/Complications ... 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 ... Signs/Symptoms/Complications ... vomiting • Late (shock ... endocrinology #peds ... #pediatrics