4 results
peds 21hydroxylasedeficiency 21ohd acromegaly diagnosis ems intraosseous io management nsfw paramedic placement praderwilli sternal syndrome treatment
Prader-Willi Syndrome: Pathogenesis and clinical findings • Maternal uniparental disomy: inheriting 2 copies of maternal chromosome
Pathogenesis and clinical ... > Neonatal and infantile ... PraderWilli #Syndrome #genetics ... #pathophysiology ... #peds #pediatrics
Sternal Intraosseous (IO) Access Placement I recently posted about the EZ-IO drill and mentioned sternal placement options
NOT to attempt live ... Well, here's a video ... NOT approved for pediatrics ... #Intraosseous #IOAccess ... #Placement #clinical
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 21-Hydroxylase Deficiency (21-OHD): Pathogenesis and Clinical Findings Autosomal recessive mutation in CYP21A2 coding for the enzyme 21-OHase
Pathogenesis and Clinical ... #21HydroxylaseDeficiency #21OHD #pathophysiology ... #genetics #endocrinology ... #peds #pediatrics
Acromegaly - Diagnosis and Management Summary - GrepMed Handbook Clinical Presentation: • Classic Acromegaly: frontal
GrepMed Handbook Clinical ... malignancy Pathophysiology ... GH stimulates liver ... phenytoin, minoxidil), genetic ... Diagnosis #Management #Endocrinology
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