Gaucher Disease - edition reliée, livre de poche

EAN (ISBN-13): 9783837411652
ISBN (ISBN-10): 3837411656
Version reliée
Date de parution: 2009
Editeur: UNI-MED, BREMEN
Poids: 0,305 kg
Langue: Englisch

Livre dans la base de données depuis 2009-12-04T20:30:24+01:00 (Zurich)
Page de détail modifiée en dernier sur 2011-11-15T15:22:06+01:00 (Zurich)
ISBN/EAN: 9783837411652

ISBN - Autres types d'écriture:
3-8374-1165-6, 978-3-8374-1165-2
Autres types d'écriture et termes associés:
Auteur du livre: gaucher, niederau
Titre du livre: gaucher

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Données de l'éditeur

Auteur: Claus Niederau
Titre: UNI-MED Science; Gaucher Disease
Editeur: UNI-MED
88 Pages
Date de parution: 2009-12-04
DE
Langue: Anglais
29,80 € (DE)
30,70 € (AT)
50,50 CHF (CH)
Not available (reason unspecified)

BB; GB; Hardcover, Softcover / Medizin/Klinische Fächer; Klinische und Innere Medizin; Medizin, Gesundheit; EA

1. Introduction 8 2. Clinical aspects 10 2.1. Classification 10 2.1.1. Non-neuronopathic form of Gaucher disease 10 2.1.2. Neuronopathic forms of Gaucher disease 11 2.2. Definitions and history 12 2.3. Aetiology and pathogenesis 13 2.4. Epidemiology 15 2.5. Natural course and prognosis 16 2.6. Classification of severity 18 3. Diagnostics 22 3.1. General symptoms 22 3.2. Medical history and clinical findings 22 3.3. Laboratory 24 3.4. Diagnostic procedures 25 3.5. Acute neuronopathic form (infantile form, type 2) 27 3.6. Enzyme measurement 28 3.7. Molecular genetic diagnosis 29 3.8. Bone manifestations in Gaucher disease 30 3.8.1. Introduction 30 3.8.2. Pathophysiology and clinical complications of bone disease 30 3.8.2.1. Skeletal complications in Gaucher disease 30 3.8.2.2. Bone mineralisation and osteoclast activity in Gaucher disease 36 3.8.2.3. Variability of bone complications in patients with Gaucher disease 36 3.8.2.4. The impact of the disease in patients with skeletal pathology 37 3.8.2.5. Skeletal pathology in children with Gaucher disease 38 3.8.3. Assessment and monitoring of skeletal pathology 38 3.8.3.1. Qualitative imaging procedures 38 3.8.3.2. Quantitative imaging procedures 39 3.8.3.3. Semiquantitative staging and classification systems 40 3.8.3.4. Assessment of skeletal pathology 41 3.8.4. Therapy of skeletal pathology 42 3.8.4.1. Response of the skeleton to enzyme replacement therapy - clinical data 42 3.8.4.2. Reconversion of the yellow bone marrow 44 3.8.5. Conclusions 44 4. Therapy 48 4.1. Enzyme replacement therapy 48 4.1.1. Historical aspects 48 4.1.2. Non-neuronopathic Gaucher disease (previously known as type 1) 50 4.1.2.1. Quality of life 50 4.1.2.2. Haematological findings 52 4.1.2.3. Hepatosplenomegaly 52 4.1.2.4. Bone changes 52 4.1.2.5. Lung involvement 53 4.1.3. Acute neuronopathic Gaucher disease (previously known as type 2) 55 4.1.4. Chronic neuronopathic course (previously known as type 3) 55 4.1.5. Special considerations for children 56 4.1.6. Dose finding 58 4.1.7. Therapy monitoring 62 4.1.8. Side effects of enzyme replacement therapy 65 4.1.9. Enzyme replacement therapy and pregnancy 65 4.2. Small molecules 66 4.2.1. Substrate reduction 66 4.2.1.1. Miglustat 66 4.2.1.2. Genz-112638 68 4.2.2. Chaperones 68 4.3. Comparison of the effect of enzyme replacement therapy (Cerezyme®) and substrate inhibition (miglustat) 70 4.4. Gene Therapy 71 4.5. Concomitant therapy 72 5. Gaucher Registry 76 6. Patient self-help groups 80 Index 86