Physical diagnosis in neonatology
Author(s)
Bibliographic Information
Physical diagnosis in neonatology
Lippincott-Raven, c1998
Available at 10 libraries
  Aomori
  Iwate
  Miyagi
  Akita
  Yamagata
  Fukushima
  Ibaraki
  Tochigi
  Gunma
  Saitama
  Chiba
  Tokyo
  Kanagawa
  Niigata
  Toyama
  Ishikawa
  Fukui
  Yamanashi
  Nagano
  Gifu
  Shizuoka
  Aichi
  Mie
  Shiga
  Kyoto
  Osaka
  Hyogo
  Nara
  Wakayama
  Tottori
  Shimane
  Okayama
  Hiroshima
  Yamaguchi
  Tokushima
  Kagawa
  Ehime
  Kochi
  Fukuoka
  Saga
  Nagasaki
  Kumamoto
  Oita
  Miyazaki
  Kagoshima
  Okinawa
  Korea
  China
  Thailand
  United Kingdom
  Germany
  Switzerland
  France
  Belgium
  Netherlands
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  United States of America
Note
Includes bibliographical references and index
Description and Table of Contents
Description
This volume is a complete and systematic guide to physical examination of neonates, interpretation of physical findings in neonates, and identification of clinical syndromes as they appear at this stage. The first section reviews the fetal and postnatal development of the various organ systems, describes techniques of physical examination, and thoroughly discusses the significance of physical findings in each body area. Coverage includes detailed information on normal findings and variations of normal, as well as abnormal findings. The second section lists the critical signs, symptoms, and physical findings that are diagnostic or suggestive of specific syndromes. Full-color photographs depict the presentation of specific syndromes in neonates
Table of Contents
- Part one Findings in the neonate: head - eye, ears, nose, oral region, neck, hair
- chest
- cardiac system
- pulmonary system
- abdomen - liver, spleen, kidney, bowel, umbilicus
- perineum - female genitalia, male genitalia, anus
- orthopaedics - hands, arms, spine, hips, legs, feet
- neuromotor - hypotonia, hypertonia, jitteriness, weakness, state, developmental, competene
- skin and subcutaneous tissue
- lymphatics. Part two Specific syndromes presentations: chromosomal disorders - Downs, Trisomy 13, Trisomy 18, Prader Willi, VATER, CHARGE, Turner/Noonan, Cornelia de Lange
- nonchromosomal disorders - infant of diabetic mother, foetal alcohol syndrome, foetal hydantoin, intrauterine compression, twin to twin transfusion, intrauterine growth retardation, hyperthyroid.
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