9 results
Cubital Tunnel Syndrome: Pathogenesis and clinical findings

 • Paresthesia of 5th and medial half of 4th
Cubital Tunnel Syndrome ... Pathogenesis and clinical ... elbow flexion test ... #Diagnosis #pathophysiology ... #signs #symptoms
Clinical features of Liver Disease in Children

#Cirrhosis #LiverFailure #Signs #Symptoms #PhysicalExam #Findings #Diagnosis #Peds #Pediatrics #Hepatology

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Clinical features ... #LiverFailure #Signs ... #Symptoms #PhysicalExam ... Findings #Diagnosis #Peds ... GrepMed Recommended Text
Clinical features of shock from dehydration in an infant

Decreased level of consciousness 
Sunken fontanelle 
Dry mucous
Clinical features ... Reduced urine output ... Extremities #PhysicalExam ... #Signs #Symptoms ... #Dehydration #Peds
Prader-Willi Syndrome: Pathogenesis and clinical findings
 • Maternal uniparental disomy: inheriting 2 copies of maternal chromosome
Prader-Willi Syndrome ... Pathogenesis and clinical ... Signs/Symptoms ... #genetics #pathophysiology ... #peds #pediatrics
Aphasia - Pathophysiology and Clinical Findings
Broca's Aphasia - Expressive language impairment: non-Fluent
 - Sensory speech areas
Aphasia - Pathophysiology ... and Clinical Findings ... Broca's Area → ↓output ... #diagnosis #signs ... #symptoms #Brocas
Wright Test (Hyperabduction Test) for Thoracic Outlet Syndrome

While measuring the radial pulses, the arm is passively
Outlet Syndrome ... development of symptoms ... #Thoracic #Outlet ... #Syndrome #clinical ... #video #physicalexam
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Wright Test (Hyperabduction Test) for Thoracic Outlet Syndrome

While measuring the radial pulses, the arm is passively
Outlet Syndrome ... development of symptoms ... #Thoracic #Outlet ... #Syndrome #clinical ... #video #physicalexam
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Cyriax Release Test for Thoracic Outlet Syndrome

Positioned behind the patient, the examiner tilt's the patient's drunk
for Thoracic Outlet ... Syndrome Positioned ... reproduces their symptoms ... #Syndrome #clinical ... #video #physicalexam
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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 ... endocrinology #peds