5 results
pediatrics diagnosis 21hydroxylasedeficiency 21ohd causes dehydration differential disease endocrinology floppy hypotonic incomplete kawasaki newborn physicalexam praderwilli shock symptoms syndrome
Clinical features of shock from dehydration in an infant Decreased level of consciousness Sunken fontanelle Dry mucous
dehydration in an infant ... Decreased level ... urine output Cold ... #PhysicalExam #Signs ... #Dehydration #Peds
Causes of Hypotonic Infant (Floppy Newborn) - Differential Diagnosis Algorithm Central Nervous System - Decreased LOC, Axial
Causes of Hypotonic Infant ... Differential Diagnosis Algorithm ... Nervous System - Decreased ... • Central Core ... #Causes #Peds #
Prader-Willi Syndrome: Pathogenesis and clinical findings • Maternal uniparental disomy: inheriting 2 copies of maternal chromosome
Prader-Willi Syndrome Signs ... , sleep apnea, cor ... PraderWilli #Syndrome #genetics ... #pathophysiology ... #peds #pediatrics
21-Hydroxylase Deficiency (21-OHD): Pathogenesis and Clinical Findings Autosomal recessive mutation in CYP21A2 coding for the enzyme 21-OHase
deficiencies present in infants ... Signs/Symptoms/Complications ... #21HydroxylaseDeficiency #21OHD #pathophysiology ... #genetics #endocrinology ... #peds #pediatrics
Evaluation of suspected incomplete Kawasaki Disease 1. AHA consensus recommendations 2. Infants ≤6 months old on day ≥7
Infants ≤6 months ... purposes of this algorithm ... lack of tapering, decreased ... clinical and lab signs ... #Diagnosis #Peds
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