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Genetic Skin Disorders
 
 

Genetic Skin Disorders [Hardcover]

Virginia P. Sybert (Author)
5.0 out of 5 stars  See all reviews (1 customer review)


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Genetic Skin Disorders (Oxford Monographs on Medical Genetics) Genetic Skin Disorders (Oxford Monographs on Medical Genetics) 5.0 out of 5 stars (1)
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Book Description

August 15, 1997 0195062183 978-0195062182 1
This book provides a comprehensive survey which details the clinical abnormalities, histopathology (including both light and electron microscopy), biochemical and molecular information, treatment, mode of inheritance and recurrence risks, prenatal diagnosis, differential diagnosis, and support for inherited dermatologic disorders. Clinicians will find the text comprehensible and practical The author has succeeded in presenting the material in a language accessible to the non-geneticist. The appendix allows physicians to quickly find the correct diagnoses to consider. The listing of specific patient support groups will be welcomed by counselors and physicians who wish to provide such information to their patients. The annotated bibliography for each entry is carefully selected to include the key reviews and pivotal papers on the subject from journals and other sources readily available to practitioners. The volume is lavishly illustrated with over 500 color and some 200 black-and-white top-quality photographs, many of which come from the author's private collection. Virginia Sybert's training and experience in both dermatology and medical genetics have been brought to bear in this volume--a lucid synthesis of information on genetic diseases of the skin. Current hypotheses and classic assumptions are presented and assessed in the light of her own clinical experience. Any physician or genetic counselor faced with a patient in whom the potential for a genetic disorder of the skin exists will find this book a practical 7ool of immense interest.


Editorial Reviews

From The New England Journal of Medicine

Dermatologists love to argue about disease taxonomy, and their efforts to define diseases over the past two centuries have relied primarily on phenotypes observable with the naked eye. That organ of detection can recognize distinctions that are more subtle than those recognized by means of the stethoscope, the x-ray, or the Petri dish -- hence, the number of recognized skin diseases is enormous. Since so many of these abnormalities "run in families," it is not surprising that diseases of the skin have been a rich lode that has not escaped the recent attention of the molecular-genetics miners. It is thus a bit surprising that until recently, the clinical focus of these interests has been summarized primarily by Butterworth and Strean's slender 1962 textbook, Clinical Genodermatology (Baltimore: Williams and Wilkins).

The paucity of book-length summaries of genetic disorders of the skin has changed markedly during the past three years with the publication of the Handbook of Genetic Skin Disorders by Novice et al. (Philadelphia: W.B. Saunders, 1994), an outline description of a comprehensive list of genodermatoses; Spitz's Genodermatoses (Baltimore: Williams and Wilkins, 1996), a photograph-figure-tabular guide with two facing pages per disease; and Moss and Savin's Dermatology and the New Genetics (Cambridge, Mass.: Blackwell Science, 1995), a 200-page compendium of diseases, also with color photographs, but arranged in a more classic textbook format with a description of each disease. These books represent major achievements, and each is authoritative and user-friendly.

Now joining this trio is Sybert's magisterial Genetic Skin Disorders, with encyclopedic discussions of more than 300 afflictions. Each description includes the requisite sections on skin and extracutaneous manifestations, inheritance, what is known of the basic defect, the differential diagnosis, and suggestions for treatment, as well as an unusually helpful annotated bibliography and an appendix listing diseases according to physical signs. But what distinguishes this work from the usual giant multiauthored good gray textbooks is the confidence bred from extensive clinical experience that is reflected in the critical commentary expressed in lively prose. For example, in describing the LEOPARD syndrome, Sybert comments, "Case reports of successful obliteration of lentigenes with dermabrasion and cryotherapy dot the literature.... I am unsure if isolated autosomal dominant multiple lentigenes exist," and the legend beneath the photograph of a patient's heavily spotted back reads, "Wall-to-wall lentigenes." It is to the credit of Oxford University Press that it has supported this personal statement, and the book is far better for the glimpses of the author's intellect.

Certainly, we cannot imagine a dermatologist or geneticist who will not buy two copies -- one for the office or clinic and one for the bedside table (we recommend one disease qhs for a year, skipping whichever Sabbath you observe) -- or a library serving clinicians that will not buy its own copy. None of us besides Dr. Sybert (or maybe the redoubtable Robert Gorlin or Victor McKusick) could possibly remember all these diseases unassisted, and in an era when the lesson of molecular genetics is that the clinicians did a pretty good job -- their lumping and splitting by and large separated fundamentally different diseases -- who could possibly make do without this information?

With the much-anticipated redefinition of inherited dermatologic diseases according to genotype rather than phenotype and the much-feared usurpation of the printed page by the World Wide Web and of the superspecialist by the generalist, this may be the end of the line for such a textbook. That's a pity, for we much prefer what we've seen of Sybertspace to what we've seen of cyberspace.

Reviewed by Ervin H. Epstein, Jr., M.D.
Copyright © 1998 Massachusetts Medical Society. All rights reserved. The New England Journal of Medicine is a registered trademark of the MMS.

Review

" This new guidebook provides an excellent means of retrieving ... information rapidly. ... very reassuring to have such a concise and thorough source of reference. This book's clear outline, excellent illustrations and diagnostic reference tables will be invaluable to paediatricians as well as clinical geneticists and dermatologists." Paediatric and Child Health (Aug 1998)

"Genetic Skin Disorders is designed to be used by basic researchers looking for an easy to use overview, and by practicing clinicians. There are over 325 conditions described in this book arranged in a hierarchy that is logical and practical....Although there are several recent, less-expensive one-volume works covering inherited skin diseases, the overall strength of this work is its ready-reference ease of use. The articals are clear and well laid out. Its margins and typeface make it easy to use....Its breadth of subject coverage, use of photographs, and concise organization makes it a useful addition to any academic or clinical library collection."--E-STREAMS

"What distinguishes this work from the usual giant multiauthored good gray textbooks is the confidence bred from extensive clinical experience that is reflected in the critical commentary expressed in lively prose...The book is far better for the glimpses of the author's intellect."--Ervin H. Epstein, Jr., MD and Michelle Aszterbaum, MD, The New England Journal of Medicine

"Virginia Sybert has done an outstanding job on her book Genetic Skin Diosrders. She has produced a useable encyclopedic volume that will be greatly appreciated by students and practitioners in dermatology, pediatrics, and genetics....this is a reader-friendly, easy-to-use reference book, which is comprehensive, informative, up-to-date, instructive, and not least of all entertaining. The author's wit and wisdom is peppered throughout the book, which entices the reader to look at "just one more section" before setting it down."--Journal of the American Academy of Dermatology

"This new guidebook provides an excellent means of retrieving...information rapidly....This book's clear outline, excellent illustrations and diagnostic reference tables will be invaluable to paediatricians as well as to clinical geneticists and dermatologists."--Paediatric Child Health Journal

"This is a comprehensive categorical compendium of genetic skin disorders. Each disorder has a differential diagnosis,clinical description, and annotated bibliography. Most have excellent photographs....This is a book that belongs in the office of every dermatologist,and in the library of every pediatric residency program next to SMITH.I recommend it without peer for dermatology board exams and recertification study. No other similar similar book has the list of support groups, therapeutic suggestions, and the annoted bibliography found here."Doody's"

Product Details

  • Hardcover: 675 pages
  • Publisher: Oxford University Press, USA; 1 edition (August 15, 1997)
  • Language: English
  • ISBN-10: 0195062183
  • ISBN-13: 978-0195062182
  • Product Dimensions: 10.2 x 7.4 x 2 inches
  • Shipping Weight: 4.8 pounds
  • Average Customer Review: 5.0 out of 5 stars  See all reviews (1 customer review)
  • Amazon Best Sellers Rank: #2,916,621 in Books (See Top 100 in Books)

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5.0 out of 5 stars This explains a lot about interrelated family health issues., October 30, 2011
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LJE "LJE" (Southwest, USA) - See all my reviews
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This review is from: Genetic Skin Disorders (Hardcover)
It was really eye-opening to learn about the many different health issues that are influenced and interrelated . A must read for family and caregivers of people with chronic, inherited skin disorders.
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Inside This Book (learn more)
First Sentence:
Genetic disorders are unique among diseases in that they affect families and generations, not just individuals. Read the first page
Key Phrases - Statistically Improbable Phrases (SIPs): (learn more)
flame nevi, bullous dermatolysis, including etretinate, sterol sulfatase deficiency, continual peeling skin, dyskeratotic comedones, aguey bouts, structural hair abnormalities, hereditary painful callosities, underlying erythroderma, systemic hyalinosis, mucoepithelial dysplasia, epidermolysis bullosa syndromes, gap junction disease, isolated pili torti, cervical hypertrichosis, nevoid hypermelanosis, eruptive vellus hair cysts, isolated white forelock, keratotic dermatosis, supersaturated saline solutions, sclerosing poikiloderma, bullous congenital ichthyosiform erythroderma, occasional parakeratosis, symmetric erythrokeratoderma
Key Phrases - Capitalized Phrases (CAPs): (learn more)
Support Group, New Fairfield, New York, University of Washington, Acta Dermatol, Birth Defects, Rector Street, Bone Joint Surg, Marie Unna, East Main, British Columbia, Ehlers-Danlos National Foundation, Mayo Clinic, South Africa, United States, Mendes da Costa, Puerto Rican, American Porphyria Foundation, Ashkenazi Jews, Ferguson Smith, Locust Street Box, Oral Pathol, Van Neste, Arch Dermatol, Cancer Res
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