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diagnosis pathophysiology endocrinology features genetics 21hydroxylasedeficiency 21ohd alzheimersdisease associated cthead decisionaid disease disorder geriatrics headinjury hiv hypothyroid kawasaki management neurocognitive
Practical Pediatric Viral Rash Algorithm Child presenting with rash and current/ recent symptoms of viral illness but
Practical Pediatric ... Viral Rash Algorithm ... current/ recent symptoms ... no signs/ symptoms ... #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 ... semantic memory ... AlzheimersDisease #Dementia ... #symptoms
Hypothyroidism – symptoms and signs. Symptoms: Tiredness/malaise, Weight gain, Anorexia, Cold intolerance, Poor memory, Change in appearance, Depression, Poor libido,
and signs. ... Symptoms: Tiredness ... intolerance, Poor memory ... slowness, Psychosis/dementia ... Carpal timel syndrome
PECARN Head CT Decision Aid The Head CT Choice decision aid was developed in Rochester, Minnesota. Full
Head CT Decision Aid ... Choice decision aid ... signs and symptoms ... #PatientInfo #Peds ... #Pediatrics #DecisionAid
Kawasaki Disease (Mucocutaneous Lymph Node Syndrome) An rare systemic acute febrile vasculitic syndrome. Aetiology unknown. Affects
febrile vasculitic syndrome ... between 6 months and ... Disease #Features #Signs ... #Symptoms #Diagnosis ... #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
HIV-Associated Neurocognitive Disorder (HAND) Definition: HIV-Associated Neurocognitive disorders categories: • Asymptomatic neurocognitive impairment • Mild neurocognitive impairment • HIV dementia Pathophysiology: HIV frequently
impairment • HIV dementia ... • Depressive symptoms ... The clinical syndrome ... neurocognitive #disorder #dementia ... #AIDS #Neurology
21-Hydroxylase Deficiency (21-OHD): Pathogenesis and Clinical Findings Autosomal recessive mutation in CYP21A2 coding for the enzyme 21-OHase
: Pathogenesis and ... Signs/Symptoms/Complications ... Labia major & minor ... endocrinology #peds ... #pediatrics
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