4 results
genetics pathophysiology 21hydroxylasedeficiency 21ohd dehydration diagnosis endocrinology infant physicalexam praderwilli screening sepsis signs symptoms syndrome
Clinical features of shock from dehydration in an infant Decreased level of consciousness Sunken fontanelle Dry mucous
Clinical features of shock ... urine output Cold ... #PhysicalExam #Signs ... #Dehydration #Peds ... #Pediatrics
Prader-Willi Syndrome: Pathogenesis and clinical findings • Maternal uniparental disomy: inheriting 2 copies of maternal chromosome
Loss of parental copy ... Prader-Willi Syndrome Signs ... , sleep apnea, cor ... 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 ... vomiting • Late (shock ... ): cold & mottled ... endocrinology #peds ... #pediatrics
Pediatrics Sepsis Screening SIGNS OF INFECTION? • Fever (>38C) • Hypothermia (<36C) • Cough/chest pain/respiratory distress •
Pediatrics Sepsis ... SEPSIS/SEPTIC SHOCK ... mottled skin, cold ... Sepsis #Screening #Pediatrics ... #peds #diagnosis
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