Atjaunināt sīkdatņu piekrišanu

E-grāmata: Signs and Symptoms of Genetic Conditions: A Handbook

Edited by (Professor of Pediatrics and Human Development at Michigan State University, Ea), Edited by , Edited by (Professor of Pediatrics, Chief of the Division of Medical Genetics, Stanford University and Lucile Packard Children's Hospital, Stanford, California, USA), Edited by
  • Formāts: 418 pages
  • Izdošanas datums: 30-May-2014
  • Izdevniecība: Oxford University Press Inc
  • Valoda: eng
  • ISBN-13: 9780199388691
  • Formāts - PDF+DRM
  • Cena: 103,86 €*
  • * ši ir gala cena, t.i., netiek piemērotas nekādas papildus atlaides
  • Ielikt grozā
  • Pievienot vēlmju sarakstam
  • Šī e-grāmata paredzēta tikai personīgai lietošanai. E-grāmatas nav iespējams atgriezt un nauda par iegādātajām e-grāmatām netiek atmaksāta.
  • Bibliotēkām
    • Oxford Medicine Online e-books
  • Formāts: 418 pages
  • Izdošanas datums: 30-May-2014
  • Izdevniecība: Oxford University Press Inc
  • Valoda: eng
  • ISBN-13: 9780199388691

DRM restrictions

  • Kopēšana (kopēt/ievietot):

    nav atļauts

  • Drukāšana:

    nav atļauts

  • Lietošana:

    Digitālo tiesību pārvaldība (Digital Rights Management (DRM))
    Izdevējs ir piegādājis šo grāmatu šifrētā veidā, kas nozīmē, ka jums ir jāinstalē bezmaksas programmatūra, lai to atbloķētu un lasītu. Lai lasītu šo e-grāmatu, jums ir jāizveido Adobe ID. Vairāk informācijas šeit. E-grāmatu var lasīt un lejupielādēt līdz 6 ierīcēm (vienam lietotājam ar vienu un to pašu Adobe ID).

    Nepieciešamā programmatūra
    Lai lasītu šo e-grāmatu mobilajā ierīcē (tālrunī vai planšetdatorā), jums būs jāinstalē šī bezmaksas lietotne: PocketBook Reader (iOS / Android)

    Lai lejupielādētu un lasītu šo e-grāmatu datorā vai Mac datorā, jums ir nepieciešamid Adobe Digital Editions (šī ir bezmaksas lietotne, kas īpaši izstrādāta e-grāmatām. Tā nav tas pats, kas Adobe Reader, kas, iespējams, jau ir jūsu datorā.)

    Jūs nevarat lasīt šo e-grāmatu, izmantojot Amazon Kindle.

Connecting an abnormal physical exam to a possible genetic condition is a daunting and inexact task for any physician, be they a primary care provider, non-geneticist specialist, or fellowship-trained geneticist.

Comprising 31 clinical protocols from the world's foremost clinical geneticists, Signs and Symptoms of Genetic Conditions provides a practical manual for the diagnosis and management of common human genetic conditions based on their presenting signs and/or symptoms. Each chapter examines a specific clinical finding and leads the user through a step-by-step approach to a differential diagnosis.

To maximize clinical utility, this handbook features:

· Prominent flow chart diagrams that graphically depict the diagnostic approach
· Concise recommendations for laboratory and/or imaging studies
· Health supervision and management strategies for the most common conditions associated with each presenting sign or symptom

Whether for the student, resident, or seasoned clinician, Signs and Symptoms of Genetic Conditions will serve as a frontline resource for navigating differential diagnosis.
Preface ix
About the Editors xi
Contributors xiii
1 Genetic Testing
1(8)
Gregory M. Enns
Louanne Hudgins
Tina M. Cowan
2 Short Stature
9(13)
Melanie A. Manning
3 Obesity
22(12)
David J. Aughton
4 Overgrowth Syndromes
34(16)
Margaret P. Adam
5 Asymmetry
50(13)
Omar A. Abdul-Rahman
6 Microcephaly
63(15)
Cynthia J. Curry
7 Macrocephaly
78(16)
Helga V. Toriello
Margaret P. Adam
8 Alterations in Cranial Shape
94(12)
Michael J. Lyons
9 Brain Malformations
106(22)
Anne Slavotinek
10 Intellectual Disability
128(8)
Agatino Battaglia
11 Autism Spectrum Disorders
136(9)
Marwan Shinawi
12 Hypotonia
145(19)
Elliott H. Sherr
Gregory M. Enns
13 Weakness
164(26)
Amy Kao
Robert D. Steiner
14 Ataxia
190(19)
Ching H. Wang
Gregory M. Enns
15 Seizures
209(26)
Randall A. Heidenreich
16 Metabolic Acidosis
235(13)
Tina M. Cowan
Gregory M. Enns
17 Hypoglycemia
248(13)
Divya Vats
Seymour Packman
18 Hyperammonemia
261(19)
Gregory M. Enns
Tina M. Cowan
19 Hepatosplenomegaly
280(25)
Renata C. Gallagher
20 Hearing Loss
305(17)
Eloise Prijoles
21 Malformations of the External Ear
322(13)
Chad Haldeman-Englert
Helga V. Toriello
22 Anomalies of the Eye
335(20)
Graeme C. Black
Rachel Gillespie
23 Facial Clefting
355(3)
Marilyn C. Jones
24 Congenital Heart Defects
358(22)
Tom Cushing
Joseph T. C. Shieh
25 Genetics of Renal Malformations
380(7)
Joseph T. C. Shieh
26 Limb Anomalies
387(33)
David B. Everman
Leslie G. Biesecker
27 Congenital Contractures: Emphasizing Multiple Congenital Contractures---Arthrogryposis
420(20)
Judith G. Hall
28 Disorders of Sexual Development
440(19)
Christopher Cunniff
29 Alterations in Skin Pigmentation
459(16)
Anna L. Bruckner
30 Skin Malformations
475(22)
Mary Beth Palko Dinulos
31 Spontaneous Abortion and Intrauterine Fetal Death
497(12)
Andrea Kwan
H. Eugene Hoyme
Index 509
Louanne Hudgins, MD, is Chief of the Division of Medical Genetics and Professor of Pediatrics at Stanford University and Lucille Packard Children's Hospital.

Helga V. Toriello, PhD, is Professor of Pediatrics and Human Development at Michigan State University and Director of Clinical Genetics at Spectrum Health.

Gregory M. Enns, MD, is Associate Professor of Pediatrics in the Division of Medical Genetics at Stanford University and Lucille Packard Children's Hospital.

H. Eugene Hoyme, MD, is Professor of Pediatrics at the Sanford School of Medicine of the University of South Dakota and Chief Academic Officer and President of Research at Sanford Health.