Özgüç Meral (ed.) Rare Diseases Integrative PPPM Approach as the Medicine of the Future

Springer, 2015. — 219 p. — (Advances in Predictive, Preventive and Personalised Medicine) — ISBN: 978-94-017-9213-4This book focuses on predictive, preventative and personalized medicine (PPPM) and how it is related to the healthcare of rare diseases. Readers will discover how advanced rare diseases healthcare provides an excellent “proof-of-principles” for the personalisation of healthcare systems on a global scale. Chapters look at national plans for rare disease, at biobanking, gene identification, rare cancers, virus gene therapy , induced pluripotency for cell therapy amongst other topics. There is a chapter dedicated to personalized medicine for hereditary deafness and another exploring the complexity of genotype-phenotype correlations. Specific diseases such as Fabry's, Gauchers and mitochondrial cytopathies are highlighted and we look at enzyme replacement therapy in lysosomal storage diseases. This work is part of a series, produced with the involvement of the European Association for Predictive, Preventive and Personalised Medicine. The series focusses on the concept of an integrative medical approach by PPPM. This volume is dedicated to all aspects related to the prediction, prevention and personalised treatments of rare diseases, and in doing so it explores developments relevant to all medical branches. The authors cover ethical considerations, the creation of a robust platform for professional communication, synergies with patient organisations, “doctor-patient” collaboration and a new philosophy of integrative medicine by PPPM. This volume serves as a reference source for scientific and medical centres in the field and can be used both at medical curricula and graduate level in the life sciences. Those who place a special emphasis on healthcare promotion and innovations intended to combat rare diseases, save the affected lives and enhance life quality will all find this book of great value.National Plans on Rare Diseases
Biobanking for Rare Diseases – Impact on Personalised Medicine
Emerging Technologies for Gene Identification in Rare Diseases
Personalized Medicine for Hereditary Deafness
Mitochondrial Diseases
Complexity of Genotype-Phenotype Correlations in Mendelian Disorders: Lessons from Gaucher Disease
Enzyme Replacement Therapy in Lysosomal Storage Diseases
Rare Cancers
Adeno-Associated Virus Gene Therapy and Its Application to the Prevention and Personalised Treatment of Rare Diseases
Induced Pluripotency for the Study of Disease Mechanisms and Cell Therapy