Neurogenetics

This book offers a practical framework for understanding neurogenetic disorders through case studies, addressing clinical assessment and management effectively.

In Neurogenetics, the authors leverage their extensive expertise in neurogenetics to offer a practical guide for understanding and managing various neurogenetic disorders. The book consists of 31 chapters that span a wide array of conditions, addressing key aspects of clinical assessment, diagnosis, and management. For many, the complexities of neurogenetics can seem daunting. This volume aims to demystify the field by equipping clinicians with a structured approach to effectively navigate these disorders.

Rather than providing an exhaustive review of every neurogenetic condition, Neurogenetics adopts a concise, case-based strategy that emphasizes the most significant and relevant disorders. Each chapter begins with a brief case study, illustrating real-life scenarios that highlight the clinical challenges faced by practitioners. This format not only enhances the book's accessibility but also ensures that it remains clinically pertinent and engaging for readers.

The scope of the book encompasses a variety of inherited disorders, including dystonia, Parkinson's disease, spastic paraplegias, mitochondrial diseases, and neuropathies, among others. The authors pay special attention to practical considerations, such as making genetic diagnoses and providing family counseling. Additionally, contemporary issues in neurogenetics, like the implications of direct-to-consumer genetic testing, are discussed, ensuring that readers stay informed about the evolving landscape of this critical field.