Genetic Steroid Disorders 2nd Edition

Genetic Steroid Disorders, 2nd Edition brings a definitive, state-of-the-art examination of steroidogenesis and its clinical consequences from a team of leading experts — Maria I. New, Bert W. O’Malley, Oksana Lekarev, Alan Parsa, Gary D. Hammer, Tony T. Yuen, and Mone Zaidi. This thoroughly updated volume translates cutting-edge genetic and molecular discoveries into practical guidance for diagnosis, management, and research.

Discover clear, clinically focused chapters that bridge molecular mechanisms and patient care, covering inherited enzyme defects, receptor abnormalities, and the full spectrum of congenital and acquired steroid disorders. Detailed discussions highlight diagnostic strategies, genotype–phenotype correlations, hormonal workups, and contemporary therapeutic approaches — all written to support endocrinologists, geneticists, pediatricians, surgeons, and clinical researchers.

What sets this second edition apart is its global relevance and multidisciplinary perspective: genetics and endocrine specialists worldwide will find actionable insights for both routine practice and complex case management. Evidence-based updates reflect the latest genomic technologies, precision-medicine approaches, and evolving treatment paradigms that matter to clinicians and investigators across North America, Europe, Asia, and beyond.

Whether you’re building a reference library, preparing lectures, or guiding patient care, this book delivers authoritative content in an accessible format. For those seeking a comprehensive resource on steroid biosynthesis disorders and their clinical implications, Genetic Steroid Disorders, 2nd Edition is an essential addition to professional collections and academic centers. Secure your copy today to stay at the forefront of endocrine genetics and improve outcomes for patients with steroid-related disorders.

Note: eBooks do not include supplementary materials such as CDs, access codes, etc.