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Craniosynostosis : Understanding and Managing the Condition: a Practical Guide for Families.

EBSCOhost Academic eBook Collection (North America) Available online

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Format:
Book
Author/Creator:
Barta, Ruth J.
Contributor:
Tveit, Cheryl.
Comstock, Heather.
Series:
Gillette Children's Healthcare Series
Language:
English
Subjects (All):
Craniosynostoses.
Neurocranial restructuring.
Physical Description:
1 online resource (250 pages)
Edition:
1st ed.
Place of Publication:
London : Gillette Children's Healthcare Press, 2024.
Summary:
This book is an in-depth guide to understanding and managing craniosynostosis, a rare condition where the bones in an infant’s skull fuse prematurely. Authored by medical professionals and parents, it provides comprehensive information on causes, symptoms, treatment options, and the emotional challenges faced by families. It combines scientific research, personal narratives, and practical insights to empower families to make informed decisions about their child’s care. Intended for parents, caregivers, and medical professionals, the book offers clarity, hope, and solidarity through detailed explanations and shared experiences. It highlights the holistic approach of Gillette Children’s and includes advancements in craniofacial surgery, making it a valuable resource for those affected by or working with craniosynostosis. Generated by AI.
Contents:
Cover Page
Praise for Craniosynostosis
Halftitle Page
Title Page
Copyright Page
Dedication
Contents
Authors and Editors
Series Foreword
Series Introduction
Chapter 1: Craniosynostosis
1.1 Introduction
1.2 Typical brain and skull development
1.3 Classifications of craniosynostosis
1.4 Prevalence, causes and risk factors, and symptoms
1.5 Diagnosis
1.6 Why treatment is important
1.7 Best practice
Key points Chapter 1
Chapter 2: Nonsyndromic craniosynostosis
2.1 Introduction
2.2 Sagittal CS
2.3 Metopic CS
2.4 Coronal CS
2.5 Lambdoid CS
2.6 Cognition, behavior, speech, and language
Key points Chapter 2
Chapter 3: Syndromic craniosynostosis
3.1 Introduction
3.2 CS syndromes Generated by AI.
Notes:
Description based on publisher supplied metadata and other sources.
Part of the metadata in this record was created by AI, based on the text of the resource.
ISBN:
9781952181108
1952181100
OCLC:
1503845202

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