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diagnosis assessment genetics neonatal symptoms 21hydroxylasedeficiency 21ohd adult brudzinskis causes cries distress endocrinology infant meningitis otitismedia painscale physicalexam postoperative praderwilli
Signs and Symptoms of Respiratory Distress Through the Years. #signs #symptoms #diagnosis #differential #neonatal #pediatrics #adult
Signs and Symptoms ... #signs #symptoms ... #diagnosis #differential ... #neonatal #pediatrics ... #adult #peds #pulmonary
Prader-Willi Syndrome: Pathogenesis and clinical findings • Maternal uniparental disomy: inheriting 2 copies of maternal chromosome
clinical findings ... • Deletion of critical ... Prader-Willi Syndrome Signs ... Syndrome #genetics #pathophysiology ... #peds #pediatrics
The infant with tachypnea or wheeze - Clinical Conditions to Consider - Bronchiolitis - Pneumonia
tachypnea or wheeze - Clinical ... increased in preterm and ... #Diagnosis #Peds ... #Pediatrics #Infant ... Tachypnea #Wheeze #Differential
Brudzinski’s Sign in Meningitis (first described in 19th century by Dr. Josef Brudzinski) Brudzinski's sign is characterized
cord movement and ... While the pathophysiology ... #Meningitis #Clinical ... #PhysicalExam #Pediatrics ... #Peds
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 CRIES is a 10-point scale, using a physiologic basis similar to APGAR: Crying; Requires increased oxygen
administration (distress ... Increased vital signs ... in the ED, the clinician ... #Diagnosis #Peds ... #Pediatrics #PainScale
Acute Otitis Media: Pathogenesis and Clinical Findings (in Children) Upper Respiratory Tract Infection: - Bacterial: Streptococcus
: Pathogenesis and ... Clinical Findings ... #OtitisMedia #pathophysiology ... diagnosis #symptoms #signs ... #peds #pediatrics
21-Hydroxylase Deficiency (21-OHD): Pathogenesis and Clinical Findings Autosomal recessive mutation in CYP21A2 coding for the enzyme 21-OHase
Clinical Findings ... Signs/Symptoms/Complications ... #21HydroxylaseDeficiency #21OHD #pathophysiology ... endocrinology #peds ... #pediatrics
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