The Calgary Guide to Understanding Disease @TheCalgaryGuide
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pathophysiology 21hydroxylasedeficiency diagnosis extraarticular genetics manifestations pediatrics peds symptoms
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
Ankylosing Spondylitis: Extra-articular Manifestations • Ocular - Inflammation of the iris, the anterior part of the
- Inflammation acute ... lung fibrosis #AnkylosingSpondylitis ... Manifestations #Complications ... pathophysiology #diagnosis #signs
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