31 results
Pyloric Stenosis - peminfographics.com
#Diagnosis #PatientInfo #Peds #Pediatrics #PyloricStenosis #Symptoms #Overview #Mnemonic
PatientInfo #Peds #Pediatrics ... PyloricStenosis #Symptoms ... #Overview #Mnemonic
SNOOP mnemonic may catch potentially life-threatening headaches
Systemic signs and disorders
Neurologic symptoms
Onset new or changed & patient
SNOOP mnemonic may ... and disorders Neurologic ... symptoms Onset ... exercise #SNOOP #mnemonic ... redflag #dangerous #neurology
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
Pituitary Mass Effects - Pathogenesis and Clinical Findings
 • Pituitary turnors are almost always a benign
A good mnemonic ... Signs / Symptoms ... endocrinology #mnemonic ... #GLFTAP #pathophysiology
Approach to Headaches - Differential Diagnosis Algorithm

Red flags (PHANTOMS):
 • Pattern change, progressively worse, papilledema
 •
) • Systemic symptoms ... Diagnosis #Algorithm #neurology ... #PHANTOMS #mnemonic
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
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