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pathophysiology genetics 21hydroxylasedeficiency 21ohd assessment childhood diagnosis evaluation febrile fever immunization praderwilli signs syndrome
The Febrile Child - some diagnostic clues to evaluating the febrile child. #Febrile #Fever #Evaluation #Assessment #Signs
some diagnostic clues ... Evaluation #Assessment #Signs ... #Symptoms #PhysicalExam ... #Diagnosis #Peds ... #Pediatrics
Prader-Willi Syndrome: Pathogenesis and clinical findings • Maternal uniparental disomy: inheriting 2 copies of maternal chromosome
Prader-Willi Syndrome Signs ... /Symptoms/Complications ... Incr Skeletal fractures ... pathophysiology #peds ... #pediatrics
Childhood Immunization Schedule: Why we immunize • Diphtheria Toxin -> URT inflammation causes pseudomembrane with hardened
Tetanus Toxin -> Spores ... hemorrhagic rash; symptoms ... lymph -> Koplik's spots ... #Immunization #peds ... #pediatrics #pathophysiology
21-Hydroxylase Deficiency (21-OHD): Pathogenesis and Clinical Findings Autosomal recessive mutation in CYP21A2 coding for the enzyme 21-OHase
enzyme 21-OHase causes ... Signs/Symptoms/Complications ... pathophysiology #genetics #endocrinology ... #peds #pediatrics
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