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Libreria medica internazionale
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Inherited Metabolic Diseases
A Clinical Approach
Hoffmann, Zschocke, Nyhan
Editore
Springer
Anno
2017
Pagine
605
ISBN
9783662494080
214,00 €
I prezzi indicati possono subire variazioni poiché soggetti all'oscillazione dei cambi delle valute e/o agli aggiornamenti effettuati dagli Editori.

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.

  • Disorders of Intermediary Metabolism

    Zschocke, Johannes

    Pages 3-8

  • Disorders of the Biosynthesis and Breakdown of Complex Molecules

    Zschocke, Johannes

    Pages 9-12

  • Neurotransmitter Defects and Related Disorders

    Hoffmann, Georg F.

    Pages 13-15

  • When to Suspect Metabolic Disease

    Nyhan, William L.

    Pages 19-28

  • Patient Care and Treatment

    Nyhan, William L. (et al.)

    Pages 29-30

  • Inherited Metabolic Diseases in the Context of Rare/Orphan Diseases

    Hoffmann, Georg F.

    Pages 31-32

  • Structured Communication and Behavioural Medicine

    Burgard, Peter

    Pages 33-40

  • Guidelines and Follow-Up

    Kölker, Stefan

    Pages 41-43

  • Patient and Family Associations

    Hannigan, Steve

    Pages 45-47

  • Adolescence, Emerging Adulthood, and Problems of Transition

    Plöckinger, Ursula

    Pages 49-60

  • Pregnancy and Maternal Care

    Murphy, Elaine

    Pages 61-80

  • Metabolic Emergencies

    Nyhan, William L. (et al.)

    Pages 81-90

  • Workup of the Patient with Metabolic Acidosis and Massive Ketosis

    Nyhan, William L. (et al.)

    Pages 91-94

  • Workup of the Patient with Lactic Acidemia: Mitochondrial Disease

    Nyhan, William L. (et al.)

    Pages 95-99

  • Work-Up of the Patient with Hypoglycemia

    Nyhan, William L. (et al.)

    Pages 101-106

  • Approach to the Child Suspected of Having a Disorder of Fatty Acid Oxidation

    Nyhan, William L. (et al.)

    Pages 107-111

  • Work-Up of the Patient with Hyperammonemia

    Nyhan, William L. (et al.)

    Pages 113-117

  • Work-Up of the Patient with Acute Neurological or Psychiatric Manifestations

    Nyhan, William L. (et al.)

    Pages 119-124

  • Emergency Treatment of Inherited Metabolic Diseases

    Nyhan, William L. (et al.)

    Pages 125-131

  • Anesthesia and Metabolic Disease

    Nyhan, William L.

    Pages 133-137

  • Principles of Dietary Management

    MacDonald, Anita

    Pages 139-153

  • Gene and Cell Therapy for Inborn Errors of Metabolism

    Harding, Cary O.

    Pages 155-171

  • Approach to the Patient with Cardiovascular Disease

    Kreuder, Joachim (et al.)

    Pages 175-201

  • Liver Disease

    Hoffmann, Georg F. (et al.)

    Pages 203-226

  • Gastrointestinal and General Abdominal Symptoms

    Kahler, Stephen G.

    Pages 227-237

  • Kidney Disease and Electrolyte Disturbances

    Nyhan, William L.

    Pages 239-250

  • Neurological Disease

    García-Cazorla, Angels (et al.)

    Pages 251-292

  • Metabolic Myopathies

    Kahler, Stephen G.

    Pages 293-312

  • Psychiatric Disease

    Mayatepek, Ertan

    Pages 313-317

  • Eye Disorders

    Burlina, Alberto (et al.)

    Pages 319-339

  • Skin and Hair Disorders

    Martinelli, Diego (et al.)

    Pages 341-370

  • The Bone in Genetic and Metabolic Diseases: A Practical Approach

    Superti-Furga, Andrea (et al.)

    Pages 371-380

  • Physical Abnormalities in Metabolic Diseases

    Moog, Ute (et al.)

    Pages 381-399

  • Hematological Disorders

    Crushell, Ellen (et al.)

    Pages 401-410

  • Immunological Problems

    Mayatepek, Ertan

    Pages 411-418

  • Newborn Screening for Inherited Metabolic Disease

    Matern, Dietrich (et al.)

    Pages 421-437

  • Biochemical Studies

    He, Miao (et al.)

    Pages 439-460

  • Enzyme Diagnostics in a Changing World of Exome Sequencing and Newborn Screening as Exemplified for Peroxisomal, Mitochondrial, and Lysosomal Disorders

    Wanders, Ronald J. A. (et al.)

    Pages 461-487

  • Molecular Genetic Analyses

    Zschocke, Johannes

    Pages 489-498

  • Family Issues, Carrier Tests and Prenatal Diagnosis

    Zschocke, Johannes

    Pages 499-503

  • Function Tests

    Zschocke, Johannes (et al.)

    Pages 505-520

  • Diagnostic Workup of Patients with Mitochondrial Diseases

    Rahman, Shamima (et al.)

    Pages 521-535

  • Pathology: Biopsy

    Radke, Josefine (et al.)

    Pages 537-550

  • Postmortem Investigations

    Rinaldo, Piero

    Pages 551-554

  • Neuroradiology

    Harting, Inga (et al.)

    Pages 555-570

 

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