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pediatrics 21hydroxylasedeficiency brudzinskis clinical diagnosis examination genetics infant meningitis newborn sign video
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 ... #genetics #endocrinology ... #peds #pediatrics
Brudzinski’s Sign in Meningitis (first described in 19th century by Dr. Josef Brudzinski) Brudzinski's sign is characterized
Brudzinski’s Sign ... flexion causes spinal ... While the pathophysiology ... Clinical #Video #PhysicalExam ... #Pediatrics #Peds
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 Newborn Infant - Routine Examination Birthweight, gestational age and birthweight percentile are noted. General observation Of the baby's
is also a late sign ... are observed for signs ... of the back and spine ... Newborn #Infant #PhysicalExam ... #Examination #Peds
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