13 results
Chaddock's Sign on Physical Exam - Babinski Equivalent
Chaddock's sign is present when stroking of the lateral
Chaddock's Sign ... sign is present ... lateral malleolus causes ... #clinical #neurology ... #Pyramidal #video
Chaddock's Sign on Physical Exam - Babinski Equivalent
Chaddock's sign is present when stroking of the lateral
Chaddock's Sign ... sign is present ... lateral malleolus causes ... #clinical #neurology ... #Pyramidal #video
Causes of Sudden Unexpected Death in Infancy (SUDI) - Differential Diagnosis Algorithm
Congenital Anomaly / Disorder:
 •
Causes of Sudden ... Unexpected Death in Infancy ... Arrhythmia • Neurologic ... Diagnosis #Algorithm #Causes ... #Peds #Pediatrics
Causes of Pediatric Constipation - Differential Diagnosis Algorithm
Dietary / Functional:
 • Insufficient Volume / Bulk
Neurologic:
 •
Causes of Pediatric ... Volume / Bulk Neurologic ... Syndrome • Muscular Dystrophy ... Diagnosis #Algorithm #Causes ... #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 sign ... this video, the infant ... #PhysicalExam #Pediatrics ... #Peds #neurology
Preterm Infant Complications - Differential Diagnosis
Respiratory:
 • Transient Tachypnea of the Newborn (TTN)
 • Respiratory Distress
Preterm Infant Complications ... Enterocolitis (NEC) Neurologic ... Preterm #Premature #Infant ... Differential #Diagnosis #Causes ... #Peds #Pediatrics
Gowers' Sign on Physical Exam

Caused by proximal muscle weakness typically seen in muscular dystrophy

#Gowers #Sign #PhysicalExam
Gowers' Sign on ... Physical Exam Caused ... #Gowers #Sign ... #PhysicalExam #neurology ... clinical #video #pediatrics
Causes of Apparent Life Threatening Event (ALTE) - Differential Diagnosis Algorithm
Cardiac:
 • Congenital Heart Disease
 •
Causes of Apparent ... Disturbances Neurologic ... Breathing • Apnea of Infancy ... Diagnosis #Algorithm #Causes ... #Peds #Pediatrics
21-Hydroxylase Deficiency (21-OHD): Pathogenesis and Clinical Findings
Autosomal recessive mutation in CYP21A2 coding for the enzyme 21-OHase
enzyme 21-OHase causes ... deficiencies present in infants ... Signs/Symptoms/Complications ... endocrinology #peds ... #pediatrics
Myasthenia Gravis Overview

Myasthenia Gravis is an autoimmune disorder of the postsynaptic neuromuscular junction.  Ab to
syndrome - Myotonic dystrophy ... test - Cogan sign ... - Peek sign ... immunosuppressants - Meds ... diagnosis #management #neurology