23 results
Woltman’s sign on Physical Exam

53-year-old man presented with fatigue and sensitivity to cold. A physical examination
Woltman’s sign on ... Woltman’s sign, ... #Woltmans #Signs ... #Clinical #Video ... #Neurology #Endocrinology
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
Woltman's Sign of Hypothyroidism oh Physical Exam

Woltman's sign is a delayed relaxation phase of an elicited
Woltman's Sign of ... is a delayed relaxation ... #Woltmans #Sign ... PhysicalExam #clinical #video ... #endocrinology
Prader-Willi Syndrome: Pathogenesis and clinical findings
 • Maternal uniparental disomy: inheriting 2 copies of maternal chromosome
Prader-Willi Syndrome Signs ... microphallus & delayed ... Syndrome #genetics #pathophysiology ... #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 ... In this video, the ... Meningitis #Clinical #Video ... PhysicalExam #Pediatrics #Peds ... #neurology
Brudzinski’s Sign in Meningitis (first described in 19th century by Dr. Josef Brudzinski)

Brudzinski's sign is characterized
Brudzinski’s Sign ... While the pathophysiology ... Video by Dr. ... Meningitis #Clinical #Video ... PhysicalExam #Pediatrics #Peds
Myoedema in Hypothyroidism on Physical Exam

Hypothyroidism is a clinical syndrome resulting from the production, secretion or
(shown in the video ... caused by the delayed ... PhysicalExam #clinical #video ... #neurology #endocrinology
Acute Otitis Media: Pathogenesis and Clinical Findings (in Children)
Upper Respiratory Tract Infection: 
 - Bacterial: Streptococcus
Respiratory syncytial virus ... #OtitisMedia #pathophysiology ... diagnosis #symptoms #signs ... #peds #pediatrics
Woltman sign - Delayed Relaxation Phase of deep tendon reflex in severe hypothyroidism

#Woltman #sign #hypothyroidism #clinical
Woltman sign - Delayed ... hypothyroidism #Woltman #sign ... hypothyroidism #clinical #video ... #endocrinology
21-Hydroxylase Deficiency (21-OHD): Pathogenesis and Clinical Findings
Autosomal recessive mutation in CYP21A2 coding for the enzyme 21-OHase
Signs/Symptoms/Complications ... #21HydroxylaseDeficiency #21OHD #pathophysiology ... #genetics #endocrinology ... #peds #pediatrics