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Produktbild: Nelson Pediatric Textbook of Rare Diseases

Nelson Pediatric Textbook of Rare Diseases Genomic Etiologies and Genetic Diagnosis

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Beschreibung

A new addition to the highly esteemed Nelson family of pediatric references, Nelson Pediatric Textbook of Rare Diseases: Genomic Etiologies and Genetic Diagnosis, edited by Drs. Robert Kliegman and Francesc (Paco) Palau, along with Associate Editors, Drs. Basel, Verbsky, Bacino, Slavotinek, Gropman,...

Beschreibung

A new addition to the highly esteemed Nelson family of pediatric references, Nelson Pediatric Textbook of Rare Diseases: Genomic Etiologies and Genetic Diagnosis, edited by Drs. Robert Kliegman and Francesc (Paco) Palau, along with Associate Editors, Drs. Basel, Verbsky, Bacino, Slavotinek, Gropman, and Rahman, provides a detailed and comprehensive guide to the diagnosis of rare disorders and the approach to undiagnosed diseases-offering in-depth content on a topic often just touched on in other pediatric textbooks. Written by the most prominent experts from around the world, this definitive text is an indispensable resource for any clinician treating pediatric patients.

  • Reflects the importance of genetic understanding and genetic diagnosis as the current approach to rare diseases
  • Organizes content around anatomical systems, with concise chapters that cover discrete disorders and conditions
  • Focuses on diagnosis and management, describing the clinical, laboratory, imaging, and genetic diagnostic features in every chapter to help differentiate disorders with similar symptoms or phenotypes
  • Contains numerous figures, algorithms, tables, photographs, and radiographic images for enhanced visual guidance
  • Includes chapters devoted to topics such as Ciliopathies, Neurodegeneration with Brain Iron Accumulation, Cancer Susceptibility Syndromes, Mitochondrial Disorders, Interferonopathies, and Epigenomic and Imprinting Syndromes, and others covering dysmorphology, neurologic, metabolic, genetic, and immune disorders
  • Shares the knowledge and experience of editors who are leaders in the field of rare diseases in both the U.S. and Europe. Among the talented editors, Dr. Palau is editor-in-chief of Orphanet Journal of Rare Diseases and the first scientific director of CIBERER, the Spanish network of excellence in rare diseases. Dr. Basel is the medical director of the Genetics and Genomics Program at Children’s Wisconsin, named a Center of Excellence by the National Organization for Rare Disorders (NORD)
  • A unique, comprehensive resource for pediatric specialists, pediatric hospitalists, pediatric fellows, geneticists, and general pediatricians, and an ideal companion volume to Nelson Pediatric Symptom-Based Diagnosis: Common Diseases and their Mimics and Nelson Textbook of Pediatrics
  • An eBook version is included with purchase. The eBook allows you to access all of the text, figures, and references, with the ability to search, make notes and highlights, and have content read aloud. Additional digital ancillary content may publish after the publication date

Produktdetails

Verkaufsrang

41845

Einband

Gebundene Ausgabe

Erscheinungsdatum

21.08.2026

Abbildungen

136 current images

Produktdetails

Verkaufsrang

41845

Einband

Gebundene Ausgabe

Erscheinungsdatum

21.08.2026

Abbildungen

136 current images

Herausgeber
Verlag Elsevier LTD
Seitenzahl

1376

Maße (L/B/H)

28,2/22,5/5,2 cm

Gewicht

3128 g

Sprache

Englisch

ISBN

978-0-443-11511-0

Herstelleradresse

Libri GmbH
Europaallee 1
36244 Bad Hersfeld
DE

Email: gpsr@libri.de

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  • Produktbild: Nelson Pediatric Textbook of Rare Diseases
  • Section I Introductory Chapters
    1. Finding the Rare Among the Common: Diagnosis, Diagnostic Error, and When to Suspect a Rare Disease
    2. Diagnostic Methods: Genomics, Omics, Biomarkers, Imaging, and Other Technologies
    3. The Approach to Rare Diseases: From Local to Global

    Section II Developmental Structural Disorders
    4. Epigenetics, Genomic Imprinting, and Imprinting Disorders
    5. Dysmorphology and Phenotyping
    6. Ciliary Signaling and Dysmorphology
    7. Ciliopathies: Clinical Presentations and Syndromes
    8. Mosaic Overgrowth Syndromes
    9. Ectodermal Dysplasia
    10. Heritable Disorders of Connective Tissue
    11. Genetic Disorders of Bone

    Section III Neuro-Sensory Disorders
    12. Rare Causes of Autistic Spectrum-Like Disorders and Syndromes With Autistic-Like Behaviors
    13. Neurodegeneration With Brain Iron Accumulation
    14. Disorders of Movement
    15. Fever-Associated Seizures and Epilepsies
    16. Nonfebrile Epilepsy Syndromes Including Epileptic Encephalopathies
    17. Hereditary Motor-Sensory Neuropathies or Charcot-Marie-Tooth Disease and Related Neuropathies
    18. Sensory and Autonomic Neuropathies Including Familial Dysautonomia and Small Fiber Neuropathies
    19. Metabolic Myopathies
    20. Skeletal Muscle Channelopathies: Periodic Paralyses and Nondystrophic Myotonias
    21. Congenital Blindness
    22. Late-Onset Blindness
    23. Sensorineural Hearing Loss

    Section IV Cardiopulmonary Disorders
    24. Interstitial Lung Diseases of Childhood
    25. Primary Ciliary Dyskinesia
    26. Pulmonary Alveolar Proteinosis
    27. Respiratory and Autonomic Disorders of Infancy, Childhood, and Adulthood (RADICA): Congenital Central Hypoventilation Syndrome (CCHS) and Rapid-Onset Obesity With Hypothalamic Dysfunction, Hypoventilation, and Autonomic Dysregulation (ROHHAD)
    28. Pediatric Cardiomyopathies
    29. Congenital/Familial Arrhythmia Syndromes
    30. Vascular and Lymphatic Malformations

    Section V Gastrointestinal and Hepatic Disorders
    31. Very Early Onset Inflammatory Bowel Disease and Congenital Diarrheal Disorders
    32. Pediatric Intestinal Pseudo-Obstruction
    33. Rare Inborn Defects Causing Malabsorption
    34. Genetic Etiologies of Neonatal and Infantile Cholestasis

    Section VI Renal Disorders
    35. Congenital Nephrotic Syndromes
    36. Bartter and Gitelman Syndromes
    37. Monogenic Etiologies of Hypertension
    38. Genetic Etiologies of Hemolytic Uremic Syndrome

    Section VII Endocrine Disorders
    39. Autoimmune Polyglandular Syndromes and Other Disorders Associated With Immune-Related Endocrinopathies
    40. Cancer Predisposition Syndromes in Children
    41. Precocious and Delayed Puberty
    42. Monogenic Diabetes: MODY and Other Rare Genetic Etiologies

    Section VIII Metabolic Disorders
    43. An Approach to Inborn Errors of Metabolism
    44. Genetic Disorders of Neurotransmitters
    45. Metabolic Crisis With Inborn Errors of Metabolism
    46. Differentiating Features of Storage Diseases
    47. Congenital Disorders of Glycosylation
    48. Mitochondrial Disorders

    Section IX Hematologic Disorders
    49. Nonimmune Hemolytic Anemias
    50. Lymphoproliferative Disorders
    51. Hereditary Bone Marrow Failure Syndromes
    52. Hereditary Etiologies of Thrombosis

    Section X Immune/Inflammatory Disorders
    53. When to Consider a Primary Immune Deficiency Disorder: Pathogens Associated With Specific Immune Defects
    54. Primary T Cell Immunodeficiencies
    55. Innate Defects in Host Defenses Against Infections
    56. Rare and Unusual Etiologies of Atopic Diseases (Eczema, Urticaria)
    57. Hereditary Autoinflammatory Disorders
    58. Type I Interferonopathies
    59. Disorders of Immune Regulation
    60. Complement Deficiencies
    61. Antibody Deficiencies