23 results
Brudzinski's Sign on Physical Exam - Meningitis

#Brudzinskis #Sign #PhysicalExam #clinical #video #neurology #peds #pediatrics #meningitis
Brudzinski's Sign ... #Brudzinskis #Sign ... #PhysicalExam #clinical ... #video #neurology ... #peds #pediatrics
Woltman’s sign on Physical Exam

53-year-old man presented with fatigue and sensitivity to cold. A physical examination
Woltman’s sign on ... reflex — Woltman’s sign ... Woltman’s sign, ... #Woltmans #Signs ... #Endocrinology
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
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 sign ... Prakash #Kernigs #Sign ... #Meningitis #Clinical ... #Peds #neurology
Sarcoidosis 
Non-caseating granulomas (Composed of T-helper & inflammatory cells) 
Clinical:
 • Disease fatal in 10% of
) Clinical: ... exertion • Neurologic ... : Bell's palsy, ... Sarcoidosis #Diagnosis #Symptoms ... #Signs #Pulmonary
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
Kawasaki Disease - Timeline of Clinical Features and Complications
 - Fever >5 days 
 - 4
Kawasaki Disease - Timeline ... of Clinical Features ... #Features #Signs ... #Symptoms #Peds ... #Pediatrics
Brudzinski's Sign on Physical Exam - Meningitis

via  @TheIntern254

#Brudzinskis #Sign #PhysicalExam #clinical #video #neurology #peds #pediatrics
Brudzinski's Sign ... #Brudzinskis #Sign ... #PhysicalExam #clinical ... #video #neurology ... #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 ... /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 ... pathophysiology #genetics #endocrinology ... #peds #pediatrics