89 results
Complications of CKD
 - Patients with stages 1-3 ([GFR] >30 mL/min) of CKD are generally asymptomatic;
Complications of ... derangements are not clinically ... #Pathophysiology ... #Nephrology #CKD ... #Complications
Brachial Plexus Lesions - Localization and Presentation

Erb palsy ("waiter's tip"), 
Klumpke palsy, 
Thoracic outlet syndrome, Winged
palsy, Thoracic outlet ... syndrome, Winged ... Comprehensive Review in Clinical ... Neurology - https
Pemberton's Sign - Thoracic Outlet Syndrome

The Pemberton maneuver is a physical examination tool used to demonstrate
Sign - Thoracic Outlet ... Syndrome The ... Pembertons #Sign #PhysicalExam ... #Clinical #Video ... Vascular #Thoracic #Outlet
Belly Dancer's Syndrome (Belly Dancer's Dyskinesia)

#Belly #Dancers #Syndrome #Dyskinesia #clinical #video #neurology #physicalexam
Belly Dancer's Syndrome ... Belly #Dancers #Syndrome ... #Dyskinesia #clinical ... #video #neurology ... #physicalexam
Prader-Willi Syndrome: Pathogenesis and clinical findings
 • Maternal uniparental disomy: inheriting 2 copies of maternal chromosome
Prader-Willi Syndrome ... Pathogenesis and clinical ... =>Prader-Willi Syndrome ... Signs/Symptoms/Complications ... #genetics #pathophysiology
Esophageal Necrosis
Etiology:
 - Ischemia and Gastric Outlet Obstruction with GERD may be inciting events
 - Associated
Ischemia and Gastric Outlet ... Stevens-Johnson syndrome ... restored to esophagus Clinical ... supportive care Complications ... common long term complication
Simultagnosia on Physical Exam (Balint Syndrome)

The patient can recognize objects one at a time but cannot
Physical Exam (Balint Syndrome ... Simultagnosia #Balint #Syndrome ... #PhysicalExam # ... clinical #video ... #neurology #ophthalmology
Marcus Gunn Phenomenon - Jaw Winking Syndrome

Jaw-winking syndrome is thought to be caused by abnormal innervation
- Jaw Winking Syndrome ... Jaw-winking syndrome ... #Jaw #Winking #Syndrome ... #clinical #video ... #neurology #physicalexam
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 ... non-arousable, decr urine output ... #21HydroxylaseDeficiency #21OHD #pathophysiology ... #genetics #endocrinology
Criss-Cross Gait on Physical Exam 

Seen in Glucose Transporter type 1 Deficiency Syndrome

#CrissCross #Criss #Cross #Gait
type 1 Deficiency Syndrome ... #Cross #Gait #PhysicalExam ... #clinical #video ... #neurology #GLUT1