Inherited Metabolic Diseases: A Clinical Approach 2nd ed
[amazon template=image&asin=3662494086]
“This volume is very timely as new genetic methods have advanced our knowledge on these diseases, on their etiology, and new therapies have been developed. … A clearly written text, with many tables and appropriate references. Highly recommended to neonatologists, geneticists, pediatricians and biochemists.” (Zvi Laron, Pediatric Endocrinology Reviews (PER), Vol. 14 (3), March, 2017)
“The editors … have assembled a talented group of contributors, with impeccable credentials in their areas of specialization. … The writing is succinct and accessible, and a remarkable amount of useful information is contained within 45 compact chapters. … The thoughtful use of tables, figures, and lists provides important details without overwhelming the non-specialist reader. … This book should be close to hand for any clinician who sees patients with inborn metabolic diseases.” (Marc Patterson, Journal of Inherited Metabolic Disease, Vol. 40, 2017)
From the Back Cover
This book focuses on clinical presentations that may be caused by inherited metabolic diseases. Its symptom- and system-based approach will help clinicians with and without detailed knowledge of human biochemistry in all specialties to reach a correct diagnosis and institute the optimal treatment program. The book summarizes the central elements of inherited metabolic diseases and describes clearly how to carry out an efficient yet complete diagnostic work-up, thereby guiding the clinician from the presenting symptoms and signs through to effective initial management. After an introduction to the different disorders, the book explains when to consider an inborn metabolic error and which initial tests to order. Core aspects such as structured communication, guidelines, transition, pregnancy, maternal care and how to respond to various medical emergencies are covered. Therapeutic concepts such as dietary treatment are delineated and practical advice provided on the quite different treatment approaches required for individual diseases. An extensive section structured according to organ systems outlines the correct approach in the context of specific symptoms and signs. The value of each of the potential investigations is explained, with precise advice on the interpretation of results. The inclusion of algorithms, tables, lists, and charts facilitates rapid decision making and information retrieval, and the appendices include a helpful guide to differential diagnosis based on clinical and biochemical phenotypes. This new updated edition of Inherited Metabolic Diseases will be an invaluable aid for the busy clinician and an excellent quick reference for metabolic and genetic specialists.