Nelson Pediatric textbook of rare diseases - genomic etiologies and genetic diagnosis

Nelson Pediatric Textbook of Rare Diseases

Genomic Etiologies and Genetic Diagnosis

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" 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,...

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Auteur(s) Robert M. Kliegman, Francesco Palau, Donald G Basel
Éditeur ELSEVIER HEALTH SCIENCES
Date 11/09/2026
Pages 850
Taille 27 x 21
Type Relié
ISBN 9780443115110

Description détaillée : Nelson Pediatric Textbook of Rare Diseases

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, Gropman, Slavotinek, Bacino, Rahman and Verbsky, 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.

  

What are the Key Features of "Nelson Pediatric Textbook of Rare Diseases" ?

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, customize your content, make notes and highlights, and have content read aloud. Additional digital ancillary content may publish up to 6 weeks following the publication date

Who are the Authors of "Nelson Pediatric Textbook of Rare Diseases" ?

Francesc (Paco) Palau : Editor-in-Chief, Orphanet Journal of Rare Diseases, CSIC Research Professor, and SJD Distinguished Investigator, Sant Joan de Déu Research Institute and Former Head, Department of Genetic and Molecular Medicine, Sant Joan de Déu Children's Hospital, Spain


Robert Kliegman : Professor and Chair Emeritus, Department of Pediatrics - Medical College of Wisconsin Nelson Undiagnosed and Rare Disease Program, USA

À PARAÎTRE OU DERNIÈRE PARUTION DANS LA MÊME CATÉGORIE :

Sommaire : 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

Auteur(s): Nelson Pediatric Textbook of Rare Diseases

Robert M. Kliegman

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