4 results
physicalexam 21hydroxylasedeficiency brudzinskis clinical diagnosis endocrinology examination infant newborn praderwilli syndrome
Brudzinski’s Sign in Meningitis (first described in 19th century by Dr. Josef Brudzinski) Brudzinski's sign is characterized
in Meningitis ( ... While the pathophysiology ... Video by Dr. ... #Video #PhysicalExam ... #Pediatrics #Peds
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 Prader-Willi Syndrome: Pathogenesis and clinical findings • Maternal uniparental disomy: inheriting 2 copies of maternal chromosome
Prader-Willi Syndrome Signs ... Infertility • Decr Bone ... PraderWilli #Syndrome #genetics ... #pathophysiology ... #peds #pediatrics
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
Newborn Infant - Routine Examination Birthweight, gestational age and birthweight percentile are noted. General observation Of the baby's
of meningitis. ... paediatrician or geneticist ... Muscle tone is assessed ... #Examination #Peds ... #Pediatrics #Diagnosis
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