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Synopsis
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.
Les informations fournies dans la section « Synopsis » peuvent faire référence à une autre édition de ce titre.
À propos de l'auteur
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
Les informations fournies dans la section « A propos du livre » peuvent faire référence à une autre édition de ce titre.
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Apert Syndrome
Edité par
Springer Nature Switzerland AG Mai 2026, 2026
ISBN 10 : 3032125502
ISBN 13 : 9783032125507
Neuf
Couverture rigide
Vendeur : BuchWeltWeit Ludwig Meier e.K., Bergisch Gladbach, Allemagne
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Buch. Etat : Neu. This item is printed on demand - it takes 3-4 days longer - Neuware -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. 672 pp. Englisch. N° de réf. du vendeur 9783032125507
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Apert Syndrome
Edité par
Springer Verlag GmbH, 2026
ISBN 10 : 3032125502
ISBN 13 : 9783032125507
Neuf
Couverture rigide
Vendeur : moluna, Greven, Allemagne
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Etat : New. Dieser Artikel ist ein Print on Demand Artikel und wird nach Ihrer Bestellung fuer Sie gedruckt. N° de réf. du vendeur 2695441601
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Apert Syndrome : Comprehensive Care of the Patient and Family
Edité par
Springer, Berlin, Department Of Plastic And Oral Surgery, Boston Children's Hospital, Springer, 2026
ISBN 10 : 3032125502
ISBN 13 : 9783032125507
Neuf
Couverture rigide
Vendeur : AHA-BUCH GmbH, Einbeck, Allemagne
Évaluation du vendeur 5 sur 5 étoiles
Buch. Etat : Neu. 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. N° de réf. du vendeur 9783032125507
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EUR 66,53
Expédition à EUR 45,99
Expédition depuis Allemagne vers Etats-Unis
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