Endocrinology Metabolism

Treat patients with hyperparathyroidism, Address specific issues of Graves' disease including thyrocardiac disease,  ophthalmopathy, dermopathy, prolonged pregnancy, mammary, Use the 2015 ATA guidelines in the management of their patients with thyroid nodules and thyroid cancer diagnosis, Determine when to do molecular genetic testing during evaluation of a thyroid nodule, Identify the commonly encountered adrenal and pituitary disorders (clinical cases), Counsel patients on fertility issues when being treated for cancer, Provide the best treatment for transgender patients, Use the new lipid lowering agents and how to manage patient who cannot take statins. Congenital adrenal hyperplasia (CAH) are any of several autosomal recessive diseases resulting from mutations of genes for enzymes mediating the biochemical steps of production of mineralocorticoids, glucocorticoids or sex steroids from cholesterol by the adrenal glands (steroid genesis).

  • Islet cell transplantation
  • Case management in multiple pituitary hormone deficiencies
  • Updated approach for the management of thyroid nodules
  • Endocrine disorders in hemoglobinopathies
  • Adrenal hyperplasia
  • Lipid metabolism by glucocorticoids

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