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  • © 2012

Inborn Metabolic Diseases

Diagnosis and Treatment

  • Being up to date: Status Quo and Trends of Treatment

  • Standard textbook in this interdisciplinary field

  • Extensively revised and updated

  • Including errors affecting adults

  • Includes supplementary material: sn.pub/extras

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Table of contents (43 chapters)

  1. Disorders of Amino Acid Metabolism and Transport

    1. Front Matter

      Pages 249-249
    2. Hyperphenylalaninaemia

      • John H. Walter, Robin H. Lachmann, Peter Burgard
      Pages 251-264
    3. Disorders of Tyrosine Metabolism

      • Anupam Chakrapani, Paul Gissen, Patrick McKiernan
      Pages 265-276
    4. Branched-chain Organic Acidurias/Acidaemias

      • Hélène Ogier de Baulny, Carlo Dionisi-Vici, Udo Wendel
      Pages 277-296
    5. Disorders of the Urea Cycle and Related Enzymes

      • Frits A. Wijburg, Marie-Cécile Nassogne
      Pages 297-310
    6. Disorders of Sulfur Amino Acid Metabolism

      • Generoso Andria, Brian Fowler, Gianfranco Sebastio
      Pages 311-321
    7. Disorders of Ornithine Metabolism

      • Matthias R. Baumgartner, David Valle
      Pages 323-332
    8. Cerebral Organic Acid Disorders and Other Disorders of Lysine Catabolism

      • Georg F. Hoffmann, Stefan Kölker
      Pages 333-347
    9. Nonketotic Hyperglycinaemia (Glycine Encephalopathy)

      • Olivier Dulac, Marie-Odile Rolland
      Pages 349-356
    10. Disorders of Proline and Serine Metabolism

      • Jaak Jaeken
      Pages 357-362
  2. Vitamin-Responsive Disorders

    1. Front Matter

      Pages 373-373
    2. Biotin-responsive Disorders

      • Matthias R. Baumgartner, Terttu Suormala
      Pages 375-384
    3. Disorders of Cobalamin and Folate Transport and Metabolism

      • David Watkins, David S. Rosenblatt, Brian Fowler
      Pages 385-402
  3. Neurotransmitter and Small Peptide Disorders

    1. Front Matter

      Pages 403-403
    2. Disorders of Neurotransmission

      • Àngels García-Cazorla, K. Michael Gibson, Peter T. Clayton
      Pages 405-422
    3. Disorders in the Metabolism of Glutathione and Imidazole Dipeptides

      • Ertan Mayatepek, Jaak Jaeken
      Pages 423-430
    4. Trimethylaminuria and Dimethylglycine Dehydrogenase Deficiency

      • Valerie Walker, Ron A. Wevers
      Pages 431-435
  4. Disorders of Lipid and Bile Acid Metabolism

    1. Front Matter

      Pages 437-437
    2. Dyslipidaemias

      • Annabelle Rodriguez-Oquendo, Peter O. Kwiterovich Jr.
      Pages 439-460

About this book

Being up to Date: Status Quo and Trends of Treatment

For those involved in the identification and management of patients with inborn errors of metabolism, this book is now recognised as the standard textbook in this interdisciplinary field. It has proved to be indispensable for professionals in specialities ranging from pediatrics, neonatology, pathological biochemistry and genetics to neurology, internal medicine, nursing, dietetics and psychology. This 5th edition has been extensively revised and updated.

What´s new

-          Additional chapter focusing on inborn errors affecting adults, particularly the late neurological presentations

-          Numerous updates on diagnostic procedures and treatment

-          Newly discovered disorders.

As with previous editions, the book opens with a section presenting the clinical approach to inborn metabolic diseases for those cases in which a diagnosis is being sought. This now includes a chapter on the clinical presentation of metabolic diseases in the older age range, using an analogous structure. If a particular diagnosis is already suspected, the reader may refer to the following sections of the book containing general chapters on diagnostic procedures and treatment, and on specific groups of disorders. As with earlier editions, the chapters have been written by authors who are internationally recognised experts on their subjects. They provide information in a clear, relevant and concise manner using a coherent structure.

Reviews

From the reviews of the fifth edition:

“The authors did an impressive job making sure the book was up to date, including discussions of therapies that are still in their experimental stages. … Inborn Metabolic Diseases is an excellent clinical guide and reference to this complex subject. It will be highly valuable to anyone who cares for patients with metabolic diseases, or for whom such diseases are regularly in the differential diagnosis.” (Daniel Kenney, Neurology, April, 2013)

“This clearly written update on a highly complex group of inherited metabolic disorders describes childhood-onset and adult-onset inherited conditions. … the book is most useful for pediatric subspecialists (e.g., clinical geneticists, neurologists), although it covers adult-onset metabolic diseases as well. … This is an outstanding book about the complex and mostly newly described field of clinical biochemical genetics. This fifth edition offers the most current overview of a rapidly evolving specialty which has relevance to all areas of medical practice.” (Hans Christoph Andersson, Doody’s Book Reviews, October, 2012)

Editors and Affiliations

  • Department of Neurology Neurometabolic Unit, Hôpital Pitié Salpêtrière 47–83 Boulevard de l’Hôpital, Paris, France

    Jean-Marie Saudubray

  • Laboratory of Physiological Chemistry de Duve Institute, University of Louvain Medical School, Brussels, Belgium

    Georges Berghe

  • Biochemical Genetics Unit Manchester Academic Health Science Centre, Central Manchester University Hospitals St Mary’s Hospital, Manchester, UK

    John H. Walter

About the editors

Professor Jean-Marie Saudubray, M.D., Director of the Metabolic/Diabetes Unit, Dep. of Pediatrics, Hopital Necker Enfants Malades, Paris, France

Professor Georges van den Berghe, Professor, Metabolic Research Group, University of Louvain Medical School, Brussels, Belgium

Dr. John H. Walter, Willink Biochemical Genetics Unit, Royal Manchester Children´s Hospital, Manchester, Great Britain

Bibliographic Information

  • Book Title: Inborn Metabolic Diseases

  • Book Subtitle: Diagnosis and Treatment

  • Editors: Jean-Marie Saudubray, Georges Berghe, John H. Walter

  • DOI: https://doi.org/10.1007/978-3-642-15720-2

  • Publisher: Springer Berlin, Heidelberg

  • eBook Packages: Medicine, Medicine (R0)

  • Copyright Information: Springer-Verlag Berlin Heidelberg 2012

  • eBook ISBN: 978-3-642-15720-2Published: 16 November 2011

  • Edition Number: 5

  • Number of Pages: XXVIII, 660

  • Topics: Pediatrics, Human Genetics, Endocrinology, Neurology

  • Industry Sectors: Biotechnology, Health & Hospitals, Pharma

Buy it now

Buying options

eBook USD 159.00
Price excludes VAT (USA)
  • Available as PDF
  • Read on any device
  • Instant download
  • Own it forever

Tax calculation will be finalised at checkout

Other ways to access