Apert Syndrome : Comprehensive Care of the Patient and Family
Language: English
Published by Springer, Berlin, Department Of Plastic And Oral Surgery, Boston Children's Hospital, Springer, 2026
- Hardcover
- New
Seller: AHA-BUCH GmbH, Einbeck, GermanyAHA-BUCH GmbH
AbeBooks seller since August 14, 2006
Condition: New
£ 57.17
Quantity: 2 available
Add to basketItem description from seller
Druck auf Anfrage Neuware - Printed after ordering - Apert syndrome - a rare genetic disorder characterized by craniofacial abnormalities, syndactyly (fusion of fingers and toes), and various health complications - presents unique challenges. Currently, there is a scarcity of educational materials dedicated to it, which hinders healthcare professionals in their quest for reliable, consolidated information - essential for accurate diagnosis and treatment. Apert syndrome's complexity demands a comprehensive approach, and by offering a resource that delves into both the medical aspects and the psychological and social dimensions, we aim to enhance the overall quality of life for individuals and families living with this condition.This unique open access text brings together a broad spectrum of topics, including the genetic basis of the syndrome, its clinical presentation, detailed diagnosis and assessment guidelines and tools, medical and surgical management strategies, insights into the psychosocial aspects of patients, and a look at future directions.Apert Syndrome is a uniquely positioned text based on a global, equitable and diverse perspective that fills a crucial knowledge gap in the understanding, diagnosis and care of individuals. It will have a profound impact on the medical and educational communities, offering invaluable insights and guidance.…
Seller Inventory # 9783032125507
- Title
- Apert Syndrome : Comprehensive Care of the Patient and Family
- Author
- John G. Meara
- Publisher
- Springer, Berlin, Department Of Plastic And Oral Surgery, Boston Children's Hospital, Springer
- Publication year
- 2026
- Condition
- Neu
- Binding
- Buch
- Language
- English
- ISBN 10
- 3032125502
- ISBN 13
- 9783032125507
- Item weight
- 1,570 grams
- Dimensions
- 254x178x35 mm
Apert syndrome - a rare genetic disorder characterized by craniofacial abnormalities, syndactyly (fusion of fingers and toes), and various health complications - presents unique challenges. Currently, there is a scarcity of educational materials dedicated to it, which hinders healthcare professionals in their quest for reliable, consolidated information - essential for accurate diagnosis and treatment. Apert syndrome's complexity demands a comprehensive approach, and by offering a resource that delves into both the medical aspects and the psychological and social dimensions, we aim to enhance the overall quality of life for individuals and families living with this condition.
This unique open access text brings together a broad spectrum of topics, including the genetic basis of the syndrome, its clinical presentation, detailed diagnosis and assessment guidelines and tools, medical and surgical management strategies, insights into the psychosocial aspects of patients, and a look at future directions.
Apert Syndrome is a uniquely positioned text based on a global, equitable and diverse perspective that fills a crucial knowledge gap in the understanding, diagnosis and care of individuals. It will have a profound impact on the medical and educational communities, offering invaluable insights and guidance.
"Synopsis" may belong to another edition of this title.
About the Author
John G. Meara, MD, DMD, MBA, Department of Plastic and Oral Surgery, Boston Children's Hospital, Boston, MA, USA
Mark Proctor, MD, Department of Neurosurgery, Boston Children's Hospital, Boston, MA, USA
Nivaldo Alonso, MD, Department of Plastic Surgery, University of São Paulo, São Paulo, Brazil
"About the title" may belong to another edition of this title.
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| Item | 7 to 10 business days | 5 to 7 business days |
|---|---|---|
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