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diagnosis pathophysiology genetics 21hydroxylasedeficiency 21ohd alzheimersdisease causes cthead decisionaid differential disease endocrinology features headinjury infancy infant inflammatory kawasaki management multisystem
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
mutations - Down syndrome ... chromosome 21) Signs ... AlzheimersDisease #Dementia ... pathophysiology #geriatrics ... #symptoms
Pediatric Inflammatory Multisystem Syndrome Temporally associated with SARS-CoV-2 infection (PIMS-TS) #PIMSTS #Pediatrics #Inflammatory #Multisystem #Syndrome #Peds #Signs
Pediatric Inflammatory ... Multisystem Syndrome ... PIMS-TS) #PIMSTS #Pediatrics ... #Multisystem #Syndrome ... #Peds #Signs #Symptoms
Kawasaki Disease (Mucocutaneous Lymph Node Syndrome) An rare systemic acute febrile vasculitic syndrome. Aetiology unknown. Affects
Mucocutaneous Lymph Node Syndrome ... febrile vasculitic syndrome ... Disease #Features #Signs ... #Symptoms #Diagnosis ... #Peds #Pediatrics
PECARN Head CT Decision Aid The Head CT Choice decision aid was developed in Rochester, Minnesota. Full
Head CT Decision Aid ... observation, and signs ... and symptoms that ... #PatientInfo #Peds ... #Pediatrics #DecisionAid
Causes of Sudden Unexpected Death in Infancy (SUDI) - Differential Diagnosis Algorithm Congenital Anomaly / Disorder: •
Differential Diagnosis Algorithm ... Sudden Infant Death Syndrome ... Differential #Diagnosis #Algorithm ... #Causes #Peds # ... Pediatrics
Prader-Willi Syndrome: Pathogenesis and clinical findings • Maternal uniparental disomy: inheriting 2 copies of maternal chromosome
Prader-Willi Syndrome ... =>Prader-Willi Syndrome ... Signs/Symptoms ... pathophysiology #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 ... Labia major & minor ... endocrinology #peds ... #pediatrics
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