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diagnosis clinical video genetics newborn symptoms 21hydroxylasedeficiency 21ohd algorithm alzheimersdisease assessment breathing brudzinskis children comparison coronavirus dementia diappers differential endocrinology
Multi-System Inflammatory Syndrome in Children (MIS-C) vs. Kawasaki Disease CDC Case Definition for MIS-C; • < 21
Multi-System Inflammatory Syndrome ... Kawasaki Disease CDC Case ... Comparison #diagnosis #peds ... #pediatrics #COVID19 ... #Inflammatory #Syndrome
The Febrile Child - some diagnostic clues to evaluating the febrile child. #Febrile #Fever #Evaluation #Assessment #Signs
some diagnostic clues ... Evaluation #Assessment #Signs ... #Symptoms #PhysicalExam ... #Diagnosis #Peds ... #Pediatrics
Paradoxical Breathing on Physical Exam Paradoxical breathing is often a sign of breathing problems. It causes the
breathing is often a sign ... It causes the chest ... Paradoxical #Breathing #PhysicalExam ... video #pulmonary #peds ... #pediatrics
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 Prader-Willi Syndrome: Pathogenesis and clinical findings • Maternal uniparental disomy: inheriting 2 copies of maternal chromosome
Prader-Willi Syndrome ... =>Prader-Willi Syndrome ... Signs/Symptoms ... #genetics #pathophysiology ... #peds #pediatrics
Causes of Urinary Incontinence - Differential Diagnosis Algorithm - Transient - Easily reversible cause (DIAPPERS)
Causes of Urinary ... Psychological/psychiatric ... Contraction - Signs ... , cauda equina syndrome ... DIAPPERS #Mnemonic #Geriatrics
Alzheimer’s Disease: Pathogenesis and Clinical Findings Risk factor for Late Onset Alzheimer's (99% of cases): - Increasing
mutations - Down syndrome ... chromosome 21) Signs ... AlzheimersDisease #Dementia #pathophysiology ... #geriatrics #diagnosis ... #signs #symptoms
Brudzinski’s Sign in Meningitis (first described in 19th century by Dr. Josef Brudzinski) Brudzinski's sign is characterized
Brudzinski’s Sign ... Passive neck flexion causes ... While the pathophysiology ... Clinical #Video #PhysicalExam ... #Pediatrics #Peds
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 Kleefstra Syndrome is a rare genetic disorder, caused by a EHMT-1 gene deletion or mutation. Most kids
Kleefstra Syndrome ... genetic disorder, caused ... and behavioural/psychiatric ... #PatientInfo #Peds ... #Pediatrics #Kleefstra
21-Hydroxylase Deficiency (21-OHD): Pathogenesis and Clinical Findings Autosomal recessive mutation in CYP21A2 coding for the enzyme 21-OHase
enzyme 21-OHase causes ... Signs/Symptoms/Complications ... #21HydroxylaseDeficiency #21OHD #pathophysiology ... endocrinology #peds ... #pediatrics
Newborn Infant - Routine Examination Birthweight, gestational age and birthweight percentile are noted. General observation Of the baby's
is also a late sign ... are observed for signs ... Newborn #Infant #PhysicalExam ... #Examination #Peds ... #Pediatrics #Diagnosis
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