Diagnosis algorithm signs table endocrinology adrenal symptoms pediatrics complications arthritis

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

21-OHD in the adrenal ... as "congenital adrenal ... Signs/Symptoms/Complications ... pathophysiology #genetics #endocrinology ... #peds #pediatrics

Rheumatoid Arthritis - Signs and Symptoms
• Ocular: Keratoconjunctivitis sicca, Episcleritis, Scleritis, Scleromalacia perforans
• Pulmonary:

Rheumatoid Arthritis ... - Signs and Symptoms ... Airways disease, Complications ... #RA #Signs #Symptoms ... #diagnosis #rheumatology

Sarcoidosis - Diagnosis and Management Summary
Epidemiology
1) High incidence in Scandinavian countries (11-24 cases per 100,000 individuals

Sarcoidosis - Diagnosis ... , and possibly renal ... Self-limiting, chronic but stable ... Extrapulmonary: ankle arthritis ... #Management #Signs

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