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Neurocutaneous Disorders
Phakomatoses & Hamartoneoplastic Syndromes
Ruggieri, Martino; Pascual Castroviejo, Ignacio; Di Rocco, Concezio (Eds.)
2008, XXI, 1070 p. 457 illus., 234 in color., Hardcover
ISBN: 978-3-211-21396-4
About this atlas
A practical, comprehensive guide to aid recognition, investigation and management of more than 60 recognized phakomatoses
An authoritative source of knowledge that bridges the gap between clinical recognition and new molecular medicine
Written by internationally renowned clinicians and researchers
Describes many recently discovered diseases for the first time
Extensively illustrated
Neurocutaneous diseases are a wide group of conditions that affect the nervous system but appear as lesions of the skin.
Some of the more common entities have variable forms of expression that can confuse the diagnosis, while for the rare conditions it is difficult to find descriptions in the literature.
Recent insights into their cellular, biochemical and molecular genetic bases have shown the essential need for a new nosology as well as updated genotype-phenotype correlations.
This book provides a practical, comprehensive guide to the recognition, investigation and management of more than 60 recognised phakomatoses, making it the most comprehensive reference work available.
Aimed primarily at clinicians and graduate researchers, this essential text bridges the gap between clinical recognition and the new molecular medicine. The problematic diagnosis of these conditions makes this comprehensive coverage essential reference material for clinicians.
The editors, distinguished clinicians and geneticists, assembled an internationally renowned group of collaborators, many of them the very same experts who first described a particular disorder or established its present accepted definition.
They have written a practical, comprehensive guide to the recognition, investigation and management of more than 60 recognised phakomatoses.
Written for:
Clinicians, researchers
Keywords:
Hypomelanosis of Ito
Neurofibromatoses
Phakomatoses
Sturge Weber Syndrome
Tuberous Sclerosis
von Hippel-Lindau Disease
von Recklinghausen's Disease
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