35 results
diagnosis signs management peds syndrome differential urology barre causes dementia genetics guillain headache hepatology msk treatment workup 21hydroxylasedeficiency 21ohd acute
Practical Pediatric Viral Rash Algorithm Child presenting with rash and current/ recent symptoms of viral illness but
Practical Pediatric ... rash and current/ recent ... symptoms of viral ... and no signs/ symptoms ... Viral #Algorithm #Pediatrics
Concussion - Acute Pathophysiology #Concussion #Pathophysiology #neurology #signs #symptoms
Concussion - Acute Pathophysiology ... #Concussion #Pathophysiology ... #neurology #signs ... #symptoms
Alzheimer’s Disease: Pathogenesis and Clinical Findings Risk factor for Late Onset Alzheimer's (99% of cases): - Increasing
chromosome 21) Signs / Symptoms ... AlzheimersDisease #Dementia #pathophysiology ... #geriatrics #diagnosis ... #signs #symptoms
Prader-Willi Syndrome: Pathogenesis and clinical findings • Maternal uniparental disomy: inheriting 2 copies of maternal chromosome
Syndrome Signs/Symptoms ... Syndrome #genetics #pathophysiology ... #peds #pediatrics
Aphasia - Pathophysiology and Clinical Findings Broca's Aphasia - Expressive language impairment: non-Fluent - Sensory speech areas
Aphasia - Pathophysiology ... deficits #Aphasia #Pathophysiology ... diagnosis #signs #symptoms ... Brocas #Wernickes #neurology
Acute Otitis Media: Pathogenesis and Clinical Findings (in Children) Upper Respiratory Tract Infection: - Bacterial: Streptococcus
#OtitisMedia #pathophysiology ... #diagnosis #symptoms ... #signs #peds #pediatrics
Refeeding Syndrome: Pathogenesis and clinical findings Patients at Risk of Refeeding Syndrome: - Little or no nutritional
nutritional intake in recent ... Syndrome #diagnosis #pathophysiology ... #symptoms #signs
Orbicularis Reflex in an Alzheimer's Patient on Physical Exam Alzheimer's is a degenerative, progressive and irreversible disease.
treated to relieve symptoms ... One of the first symptoms ... of memory for recent ... clinical #video #neurology
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 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 ... endocrinology #peds #pediatrics
Primary Biliary Cirrhosis (PBC) - Summary PBC Epidemiology: • Female:Male 9:1 • Common European descent • Age:
Common European descent ... 65 years PBC Pathophysiology ... PBC Signs and Symptoms
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