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genetics 21hydroxylasedeficiency cries endocrinology neonatal otitismedia painscale postoperative praderwilli symptoms syndrome
21-Hydroxylase Deficiency (21-OHD): Pathogenesis and Clinical Findings Autosomal recessive mutation in CYP21A2 coding for the enzyme 21-OHase
Pathogenesis and Clinical ... Signs/Symptoms/Complications ... #pathophysiology ... endocrinology #peds ... #pediatrics
Prader-Willi Syndrome: Pathogenesis and clinical findings • Maternal uniparental disomy: inheriting 2 copies of maternal chromosome
Pathogenesis and clinical ... Prader-Willi Syndrome Signs ... delayed puberty -> Infertility ... Syndrome #genetics #pathophysiology ... #peds #pediatrics
CRIES is a 10-point scale, using a physiologic basis similar to APGAR: Crying; Requires increased oxygen
Increased vital signs ... in the ED, the clinician ... #Diagnosis #Peds ... #Pediatrics #PainScale ... PostOperative #Assessment
Acute Otitis Media: Pathogenesis and Clinical Findings (in Children) Upper Respiratory Tract Infection: - Bacterial: Streptococcus
Pathogenesis and Clinical ... #OtitisMedia #pathophysiology ... #diagnosis #symptoms ... #signs #peds #pediatrics
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