图书简介

1. Introduction 2. Adrenal Development 3A. Congenital Adrenal Hyperplasia Owing to 21 Hydroxylase Deficiency 3B. Growth Hormone Therapy to Improve Adult Height in Patients with Congenital Adrenal Hyperplasia 3C. Bone Mineral Density and Skeletal Outcomes in Congenital Adrenal Hyperplasia 3D. Steroid 11B-Hydroxylase Deficiency and Related Disorders 3E. 3B-Hydroxysteroid Dehydrogenase Deficiency 3F. Genetic Deficiencies for Cytochrome P450 (CYP17A1): Combined 17 Hydroxylase/17,20 Lyase Deficiency and Isolated 17,20 Lyase Deficiency 4. Disorders in the Initial Steps in Steroidogenesis 5. P450 Oxidoreductase Deficiency (PORD) 6. Aromatase Deficiency 7. 46XY DSD due to 17bHydroxysteroid Dehydrogenase 3 Deficiency 8A. Steroid 5a-Reductase 2 Deficiency 8B. Marsupial Pathway of Steroid 5a Reductase Deficiency in Humans 9. Androgen Insensitivity Syndrome 10. Persistent Mullerian Duct Syndrome 11A. Apparent Mineralocorticoid Excess (AME) 11B. History, Biology, Pathophysiology of AME 11C. Primary Aldosteronism: Where are we now? 12. Nuclear Receptor Co-regulators 13. Genetics of Adrenal Tumors 14. Genetic Factors in Cushing Disease Pathogenesis 15. The Genetics of Ovotesticular Disorders of Sexual Development 16A. Impact of Genetic Steroid Disorders on Human Fertility 16B. Ambiguous Genitalia in Newborns 16C. Prenatal Diagnosis of Congenital Adrenal Hyperplasia 16D. Preimplantation Diagnosis of Congenital Adrenal Hyperplasia 17. Psychoendocrinology of Congenital Adrenal Hyperplasia 18. Treatment and Outcome of Congenital Adrenal Hyperplasia: Current Reconstructive Surgery 19. Debates and Controversies in Genetic Steroid Disorders 20. Geographical Endocrinology of Genetic Steroid Disorders 21. Animal Models of Adrenal Steroid Disorders 22A. Case Reports: Extreme Presentations from Inactivation and Hyperactivation of the LH receptor (LHCGR) action 22B. Case Reports: Unsolved Mysteries of Steroid Disorders

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