b12 peds video sign diagnosis infant pathophysiology symptoms orthopedics pediatrics - GrepMed

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2 results

21-Hydroxylase Deficiency (21-OHD): Pathogenesis and Clinical Findings
Autosomal recessive mutation in CYP21A2 coding for the enzyme 21-OHase

deficiencies present in infants ... Signs/Symptoms/Complications ... #21HydroxylaseDeficiency #21OHD #pathophysiology ... endocrinology #peds ... #pediatrics

Acute Otitis Media: Pathogenesis and Clinical Findings (in Children)
Upper Respiratory Tract Infection:
- Bacterial: Streptococcus

#OtitisMedia #pathophysiology ... #diagnosis #symptoms ... #signs #peds #pediatrics

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