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treatment 21hydroxylasedeficiency 21ohd causes differential genetics hematology nephrology pathophysiology peds pheochromocytoma polycythemiavera pv rhabdomyolysis sarcoidosis summary
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
Polycythemia Vera (PV) - Diagnosis and Management Summary Diagnostic Criteria: • Elevated hemoglobin and/or hematocrit AND •
and Management ... Summary Diagnostic ... , signs, and complications ... • Treatment algorithms ... #Management #Summary
Rhabdomyolysis - Differential Diagnosis Framework and Management Summary Causes of Rhabdomyolysis: • Trauma: - Immobilization - Crush injury - Compartment
- Differential Diagnosis ... Framework and Management ... : • Triad of symptoms ... HAGMA • Late complication ... #Management #causes
Pheochromocytoma - Diagnosis and Management Summary 10 percent rule = 10% of pheochromocytomas are extra-adrenal, multiple, bilateral,
pheochromocytomas are extra-adrenal ... bilateral, malignant, pediatric ... life • M=F Symptoms ... and Signs: 50% ... and signs: •
Sarcoidosis - Diagnosis and Management Summary Epidemiology 1) High incidence in Scandinavian countries (11-24 cases per 100,000 individuals
Sarcoidosis - Diagnosis ... and Management ... , and possibly renal ... Self-limiting, chronic but stable ... #Management #Signs
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