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Introduction
Clinical Diagnosis of Endocrine Hypertension
Primary aldosteronism
Pheochromocytoma
Congenital adrenal hyperplasia: 11beta-hydroxylase deficiency
Congenital adrenal hyperplasia: 17alpha-hydroxylase deficiency
Apparent mineralocorticoid excess
Constitutive activation of the mineralocorticoid receptor (Geller syndrome)
Liddle syndrome
Pseudohypaldosteronism type 2
Insulin Resistance
Hyperparathyroidism
Cushing’s Syndrome
Glucocorticoid Resistance
Hyperthyroidism
Hypothyroidism
Acromegaly