Connective Tissue and Its Heritable Disorders : Molecular, Genetic, and Medical Aspects ISBN: 9780471221920 Platform/Publisher: WOL / John Wiley & Sons, Ltd Digital rights:Users: Unlimited; Printing: Unlimited; Download: Unlimited Subjects: Medicine; General & Introductory Medical Science;
The Second Edition of Connective Tissue and Its Heritable Disorders: Molecular, Genetic, and Medical Aspects is the definitive reference text in its field, with over 40% more pages on the nature, diagnosis, and treatment of disease than its predecessor. Collecting new research on disorders detailed in the first edition as well as on those previously excluded, editors Peter Royce and Beat Steinmann provide the most up-to-date clinical and scientific information for medical specialists treating affected individuals. Features of this revised and updated volume include detailed reviews of the clinical diagnosis, mode of inheritance, risk of recurrence, and prenatal diagnosis of each inherited connective tissue disorder; a thorough description of the morphology of connective tissues; a completely updated and revised section on the biology of the extracellular matrix; and the addition of syndromes such as craniosyntosis, and disorders of sulfate metabolism.
Peter M Royce received his Ph.D. at Cambridge University in the 1970s, and has held research and teaching positions in academic and industrial research institutes in England, Australia, Switzerland, and Japan. He currently works in Cambridge as a writer and consultant.
Beat Steinmann trained as a pediatrician at the University of Zurich, specializing in inborn errors of metabolism. He was the first to describe mutations in collagen I in patients with Ehlers-Danlos syndrome and lethal osteogenesis imperfecta. He is currently a Full Professor and Head of the Division of Metabolism and Molecular Pediatrics, Department of Pediatrics, in the University of Zurich. He is also editor of the European Journal of Pediatrics , and editor for the section Heritable Disorders of Connective Tissues in Online Mendelian Inheritance in Man (OMIM) .
