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pediatrics genetics 21hydroxylasedeficiency 21ohd brudzinskis cop cryptogenic diagnosis management meningitis organizing pneumonia praderwilli syndrome video
Prader-Willi Syndrome: Pathogenesis and clinical findings • Maternal uniparental disomy: inheriting 2 copies of maternal chromosome
Pathogenesis and clinical ... Loss of parental copy ... Prader-Willi Syndrome Signs ... sleep apnea, cor pulmonale ... #peds #pediatrics
Brudzinski’s Sign in Meningitis (first described in 19th century by Dr. Josef Brudzinski) Brudzinski's sign is characterized
causes spinal cord ... While the pathophysiology ... #Meningitis #Clinical ... #Video #PhysicalExam ... #Pediatrics #Peds
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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 ... Signs/Symptoms/Complications ... #21HydroxylaseDeficiency #21OHD #pathophysiology ... #genetics #endocrinology ... #peds #pediatrics
Cryptogenic Organizing Pneumonia - Illness Script PATHOPHYSIOLOGY: Unknown trigger, reversible inflammatory/fibroproliferative process. Polypoid fibroblastic aggregates that plug
Illness Script PATHOPHYSIOLOGY ... Males=Females SIGNS ... DIAGNOSTICS: Clinical ... TylerLarsenMD #COP ... diagnosis #management #pulmonary
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