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pathophysiology 21hydroxylasedeficiency 21ohd benign bph cah congenital cushings deficiency endocin genetics gravesdisease hydroxylase hypercortisolism management pediatrics peds prostate prostatic sarcoidosis
Congenital Adrenal Hyperplasia - 21-Hydroxylase Deficiency - Signs and Symptoms • Brain: Androgenization effects, Glucocorticoid effects,
Hydroxylase Deficiency - Signs ... and Symptoms • ... #Deficiency #Signs ... #Symptoms #diagnosis ... #endocrinology
Graves’ Disease: Pathogenesis and Clinical Findings B & T lymphocyte mediated autoimmunity attack TSH receptor -> Continuous
Pathogenesis and Clinical ... Thyroid gland hyperplasia ... pathophysiology #endocin #endocrinology ... #symptoms #signs ... #diagnosis
21-Hydroxylase Deficiency (21-OHD): Pathogenesis and Clinical Findings Autosomal recessive mutation in CYP21A2 coding for the enzyme 21-OHase
Pathogenesis and Clinical ... 21-OHD in the adrenal ... hyperplasia". ... Signs/Symptoms/Complications ... pathophysiology #genetics #endocrinology
Cushing's Syndrome - Hypercortisolism - Diagnosis and Clinical Features 1) Skin • Thin, easily bruisable skin with
and Clinical Features ... cortex contralateral ... shows bilateral hyperplasia ... #signs #symptoms ... #endocrinology
Benign Prostatic Hyperplasia: Pathogenesis and Clinical Findings Hormonal alterations (result of aging process) ->
Benign Prostatic Hyperplasia ... Pathogenesis and Clinical ... Acute or chronic renal ... Pathophysiology #Urology #Signs ... #Symptoms #Diagnosis
Sarcoidosis - Diagnosis and Management Summary Epidemiology 1) High incidence in Scandinavian countries (11-24 cases per 100,000 individuals
Sarcoidosis - Diagnosis ... , and possibly renal ... failure Clinical ... anterior/posterior MSK ... #Management #Signs
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