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pathophysiology 21hydroxylasedeficiency 21ohd cthead decisionaid diagnosis elbow endocrinology fracture headinjury msk patientinfo pecarn praderwilli radialhead radiology radius syndrome xray
Prader-Willi Syndrome: Pathogenesis and clinical findings • Maternal uniparental disomy: inheriting 2 copies of maternal chromosome
Prader-Willi Syndrome Signs ... /Symptoms/Complications ... PraderWilli #Syndrome #genetics ... pathophysiology #peds ... #pediatrics
PECARN Head CT Decision Aid The Head CT Choice decision aid was developed in Rochester, Minnesota. Full
observation, and signs ... and symptoms that ... (Figure 2) #Management ... #PatientInfo #Peds ... #Pediatrics #DecisionAid
RADIAL HEAD FRACTURE Radial head fractures are the most common elbow fracture in adults and are
anterior sail sign ... injury, elbow dislocation ... fracture • ED Management ... II-IV, pending orthopedic ... #Orthopedics #MSK
21-Hydroxylase Deficiency (21-OHD): Pathogenesis and Clinical Findings Autosomal recessive mutation in CYP21A2 coding for the enzyme 21-OHase
Signs/Symptoms/Complications ... pathophysiology #genetics ... endocrinology #peds ... #pediatrics
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