16 results
Parkinson's Disease - Signs and Symptoms
Systemic: Tremor and Slowness, Impaired balance, Small Handwriting, Sleepiness, Trouble Moving
Parkinson's Disease - Signs ... Walking, Masked Face Central ... Muscular: Weakness ... Parkinsons #Disease #Signs ... #Symptoms #neurology
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 ... position with the hip and ... #PhysicalExam #Pediatrics ... #Peds #neurology
Characteristics of Peripheral and Central Vertigo
PERIPHERAL VERTIGO
 • Onset: Sudden
 • Intensity: Severe initially, often decreasing
Central Vertigo ... labyrinthitis) CENTRAL ... or minutes with vascular ... #signs #symptoms ... #comparison #neurology
Diagnostic Algorithm for Dizziness and Vertigo
Peripheral Vertigo:
 • Attacks: Sudden, severe, can last anywhere from seconds
Varies • No neurologic ... present Central ... or minutes with vascular ... position change • Neurologic ... differential #diagnosis #neurology
Causes of Dizziness - Vertigo - Differential Diagnosis Algorithm
True Vertigo - Illusion of Rotary Movement
Peripheral Vestibular
Bone Fracture Central ... Dysfunction - Imbalance, neurologic ... symptoms/signs, ... Glomus Tumors - Vascular ... Dizziness #Vertigo #Neurology
THE LIMPING OR NON-WEIGHT BEARING CHILD PATHWAY

RED FLAGS - In all cases there are specific
markers which
severe disease and ... local guidelines General ... splenomegaly, abnormal neurology ... Pathway #Child #Peds ... #Pediatrics #Diagnosis
Acute Spinal Cord Injuries: Pathogenesis and clinical findings
 • Anterior Cord Syndrome -> Anterior spinal artery
clinical findings ... injury, often from vascular ... mimics complete • Central ... pathophysiology #signs ... #orthopedics #neurology
Multiple Sclerosis - Summary

Multiple Sclerosis (MS) is an autoimmune-mediated neurodegenerative disease of the central nervous system
disease of the central ... /SYMPTOMS: • CENTRAL ... Signs and symptoms ... Laboratory findings ... diagnosis #management #neurology
21-Hydroxylase Deficiency (21-OHD): Pathogenesis and Clinical Findings
Autosomal recessive mutation in CYP21A2 coding for the enzyme 21-OHase
: Pathogenesis and ... Clinical Findings ... Signs/Symptoms/Complications ... endocrinology #peds ... #pediatrics
Galant Reflex on Physical Exam

The Galant reflex is present at birth and remains until the 2nd
present at birth and ... pelvis is pulled up and ... of the flexor control ... clinical #video #Neurology ... #Peds #Pediatrics