Apert Syndrome
Comprehensive Care of the Patient and Family
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Beschreibung
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.
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.
A unique, comprehensive book on the medical and surgical management of Apert Syndrome Combines current understanding, cutting-edge research, global perspective and a patient-oriented approach Presents genetics, clinical presentation, diagnosis, management, psychosocial aspects and future directions This is an open access book
Autor*in
John G. Meara
Themen in »Apert Syndrome«
Apert syndrome cranial surgery craniofacial surgery maxillofacial surgery syndactyly surgery genetic disorder craniofacial abnormality hydrocephalus monobloc hypertelorism Open Access