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diagnosis peds disease assessment features mentalstatus pathophysiology score slums 21hydroxylasedeficiency 21ohd alzheimersdisease cirrhosis endocrinology findings genetics hepatology incomplete liverfailure mse
The Mini-Mental State Examination (MMSE) is commonly used as a screening tool to detect dementia. However,
Mini-Mental State Examination ... tool to detect dementia ... for orientation, memory ... #Diagnosis #Geriatrics ... #Dementia #SLUMS
Kawasaki Disease (Mucocutaneous Lymph Node Syndrome) An rare systemic acute febrile vasculitic syndrome. Aetiology unknown. Affects
Kawasaki Disease ... #Kawasaki #Disease ... #Features #Signs ... #Symptoms #Diagnosis ... #Peds #Pediatrics
Practical Pediatric Viral Rash Algorithm Child presenting with rash and current/ recent symptoms of viral illness but
Practical Pediatric ... Viral Rash Algorithm ... five days and no signs ... / symptoms of sepsis ... #Pediatrics #Peds
Alzheimer’s Disease: Pathogenesis and Clinical Findings Risk factor for Late Onset Alzheimer's (99% of cases): - Increasing
chromosome 21) Signs ... AlzheimersDisease #Dementia ... pathophysiology #geriatrics ... #diagnosis #signs ... #symptoms
SLU Mental Status Examination Tool What does the SLU Mental Status Exam Test Do? Q1-Q3: Attention, immediate recall,
Mental Status Examination ... registration Q6: Memory ... extrapolation #Diagnosis #Geriatrics ... #Dementia #SLUMS ... #MentalStatus #Examination
Kawasaki Disease - Timeline of Clinical Features and Complications - Fever >5 days - 4
Kawasaki Disease ... Extremities #Kawasaki ... Timeline #Features #Signs ... #Symptoms #Peds ... #Pediatrics
Evaluation of suspected incomplete Kawasaki Disease 1. AHA consensus recommendations 2. Infants ≤6 months old on day ≥7
suspected incomplete Kawasaki ... purposes of this algorithm ... clinical and lab signs ... Diagnosis #Peds #Pediatrics ... #Kawasaki #Disease
Clinical features of Liver Disease in Children #Cirrhosis #LiverFailure #Signs #Symptoms #PhysicalExam #Findings #Diagnosis #Peds #Pediatrics #Hepatology **
#LiverFailure #Signs ... #Symptoms #PhysicalExam ... Diagnosis #Peds #Pediatrics ... Guide to Physical Examination
21-Hydroxylase Deficiency (21-OHD): Pathogenesis and Clinical Findings Autosomal recessive mutation in CYP21A2 coding for the enzyme 21-OHase
Signs/Symptoms/Complications ... Labia major & minor ... endocrinology #peds #pediatrics
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