4 results
pediatrics diagnosis genetics signs 21hydroxylasedeficiency 21ohd endocrinology lupus manifestations mucocutaneous otitismedia praderwilli sle syndrome
Prader-Willi Syndrome: Pathogenesis and clinical findings • Maternal uniparental disomy: inheriting 2 copies of maternal chromosome
Syndrome Signs/Symptoms ... /Complications: ... Syndrome #genetics #pathophysiology ... #peds #pediatrics
Acute Otitis Media: Pathogenesis and Clinical Findings (in Children) Upper Respiratory Tract Infection: - Bacterial: Streptococcus
resolve by 72 hours Complications ... slide for full mechanisms ... #OtitisMedia #pathophysiology ... #diagnosis #symptoms ... #signs #peds #pediatrics
Lupus (SLE): Mucocutaneous Manifestations • Langerhan cells and keratinocytes release cytokines -> localized inflammatory response ->
inflammation (complex mechanism ... Manifestations #pathophysiology ... diagnosis #signs #symptoms ... #complications
21-Hydroxylase Deficiency (21-OHD): Pathogenesis and Clinical Findings Autosomal recessive mutation in CYP21A2 coding for the enzyme 21-OHase
Signs/Symptoms/Complications ... #21HydroxylaseDeficiency #21OHD #pathophysiology ... endocrinology #peds
No results found for "SlowMotion choreiform mechanism pathophysiology symptoms complications peds"
Try removing search terms or sorting by relevance
Or Upload an image for you and others searching for #SlowMotion #choreiform #mechanism #pathophysiology #symptoms #complications #peds