Inherited metabolic diseases : a clinical approach /

Inherited metabolic diseases : a clinical approach /

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Bibliographic Details
Uniform title:Inherited metabolic diseases (Springer)
Edition:Second edition.
Imprint:Heidelberg : Springer, [2017]
©2017
Description:1 online resource (xviii, 605 pages) : illustrations (some color)
Language:English
Subject:
Metabolism, Inborn errors of -- Diagnosis.
Metabolism -- Disorders -- Genetic aspects.
Metabolism, Inborn Errors -- diagnosis.
Metabolism, Inborn Errors -- genetics.
Metabolism, Inborn Errors -- therapy.
Metabolism, Inborn errors of -- Diagnosis.
Format: E-Resource Book
URL for this record:http://pi.lib.uchicago.edu/1001/cat/bib/11266816
Hidden Bibliographic Details
Other uniform titles:Preceded by: Inherited metabolic diseases.
Other authors / contributors:Hoffmann, Georg F. (Georg Friedrich), editor.
Zschocke, Johannes, editor.
Nyhan, William L., 1926- editor.
ISBN:9783662494103
3662494108
9783662494080
3662494086
Digital file characteristics:text file
PDF
Notes:Revised edition of: Inherited metabolic diseases : a clinical approach / edited by Georg F. Hoffmann, Johannes Zschocke, William L. Nyhan. ©2010.
Includes bibliographical references and index.
Online resource; title from pdf title page (SpringerLink, viewed March 21, 2017).
Summary:"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"--Publisher's description
Other form:Print version: Inherited metabolic diseases. Second edition. Berlin : Springer, [2017] 9783662494080
Standard no.:10.1007/978-3-662-49410-3
Table of Contents:
  • Introduction to inborn errors of metabolism: disorders of intermediary metabolism
  • Mitochondriopathies neurotransmitter defects
  • Disorders of the biosynthesis and breakdown of complex molecules. Approach to the patient: when to suspect metabolic disease
  • Patient care and treatment
  • Metabolic emergencies
  • Anesthesia and metabolic disease
  • Principles of dietary therapy
  • Principles of enzyme replacement therapy
  • Principles of gene therapy. Organ systems in metabolic disease: cardiovascular disease
  • Liver disease
  • Gastrointestinal and general abdominal symptoms
  • Kidney disease and electrolyte disturbances
  • Neurological disease
  • Metabolic myopathies
  • Psychiatric disease
  • Eye disorder
  • Skin and hair disorders
  • Bone disorders
  • Physical abnormalities in metabolic diseases
  • Hematological disorders
  • Immunological problems. Investigations for metabolic diseases: newborn screening
  • Biochemical studies
  • Enzymes, metabolic pathways, flux control analysis and the enzymology of specific groups of inherited metabolic diseases
  • Molecular investigations (DNA studies)
  • Pathology / Biopsy
  • Postmortem investigations
  • Neuroimaging
  • Function tests
  • Suspected mitochondrial disorder. Appendix: differential diagnosis of clinical and biochemical phenotypes.

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