Fanconi anemia (FA) is a rare genetic disease discovered 80 years ago by Guido Fanconi, an eminent Swiss pediatrician. It is characterized by short stature, skeletal anomalies, increased incidence of solid tumors and leukemias, bone marrow failure and cellular sensitivity to DNA damaging agents. Following a historical account, exemplary case reports and the current status of FA genes and their mutations, this volume discusses neoplasia in FA as well as current approaches to pre- and postnatal diagnosis. Further topics include revertant mosaicism as a kind of 'natural gene therapy' and hematopoietic stem cell transplantation as the only curative approach in FA. The final chapters investigate evolutionary aspects of the FA genes with special emphasis on the avian genome and the involvement of FA genes in recombinational types of DNA repair. Physicians and researchers in the fields of pediatrics, hematology, cancer, genetics, DNA repair and aging will benefit from understanding this disease, which illustrates the complex network of genomic maintenance systems that protect us from cancer and premature aging.

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Yes, you can access Fanconi Anemia by Schmid, Schindler, Hoehn in PDF and/or ePUB format, as well as other popular books in Medicine & Pediatric Medicine. We have over one million books available in our catalogue for you to explore.

Information

Publisher

S. Karger

Year

2007

ISBN

9783318014617

Edition

Topic

Medicine

Subtopic

Pediatric Medicine

Cover
Contents
Editorial
Preface
Introductory Remarkss
Author Index
Subject Index