Congenital Craniofacial Deformities: Genetic and Clinical Aspects PDF Download
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Author: Hanyao Huang
Publisher: Frontiers Media SA
ISBN: 2832537456
Category : Medical
Languages : en
Pages : 79
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Book Description
Author: Hanyao Huang
Publisher: Frontiers Media SA
ISBN: 2832537456
Category : Medical
Languages : en
Pages : 79
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Book Description
Author: Richard Merle Goodman
Publisher:
ISBN:
Category : Medical
Languages : en
Pages : 608
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Book Description
Author: Michel Stricker
Publisher:
ISBN:
Category : Medical
Languages : en
Pages : 616
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Book Description
This work covers craniofacial malformations and growth, and their treatment, surgery and classification. Written for practising plastic surgeons and maxillofacial surgeons, it should also be of interest to oral and ENT surgeons and orthodontists.
Author:
Publisher: Alan R. Liss
ISBN:
Category : Medical
Languages : en
Pages : 244
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Book Description
Author: Ulrich Meyer
Publisher: Springer Nature
ISBN: 303046024X
Category : Medical
Languages : en
Pages : 393
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Book Description
This is the first volume in an interdisciplinary three-book series covering the full range of biological, clinical, and surgical aspects in the evaluation, diagnosis, and treatment of patients with craniofacial malformations. This volume opens by considering general topics such as developmental biology and disease classification and then examines in depth the biological basis of the various malformations, including craniosynostoses, cleft-lip and palate with complex orofacial clefts, branchio-oculo-facial syndromes, rare syndromes, soft tissue malformations, and dysgnathia. Psychological aspects, including psychological evaluation methods and therapies and quality of life issues, are then addressed. Finally, all relevant clinical, radiological, and genetic investigations are described and important diagnostic issues are explored. Featuring numerous high-quality illustrations, the book will be of high value for all clinicians, researchers, and postgraduate students who deal with these malformations. The accompanying two volumes describe treatment principles and present in an atlas manner all relevant surgical techniques in detail. The content of this multivolume set, written by the world’s leading research and clinical specialists in their discipline, represents therefore the recent intellect, experience, and state of this medical field.
Author: Peter Thorogood
Publisher:
ISBN:
Category : Bones
Languages : en
Pages : 274
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Book Description
Author: Mary Ellen McCann
Publisher: Cambridge University Press
ISBN: 1107069777
Category : Medical
Languages : en
Pages : 465
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Book Description
A practical, comprehensive guide to the special needs of infants and neonates undergoing anesthesia.
Author:
Publisher: Elsevier
ISBN: 0444543007
Category : Medical
Languages : en
Pages : 273
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Book Description
Down syndrome (DS) is the most common example of neurogenetic aneuploid disorder leading to mental retardation. In most cases, DS results from an extra copy of chromosome 21 (HSA21) producing deregulated gene expression in brain that gives raise to subnormal intellectual functioning. The topic of this volume is of broad interest for the neuroscience community, because it tackles the concept of neurogenomics, that is, how the genome as a whole contributes to a neurodevelopmental cognitive disorders, such as DS, and thus to the development, structure and function of the nervous system. This volume of Progress in Brain Research discusses comparative genomics, gene expression atlases of the brain, network genetics, engineered mouse models and applications to human and mouse behavioral and cognitive phenotypes. It brings together scientists of diverse backgrounds, by facilitating the integration of research directed at different levels of biological organization, and by highlighting translational research and the application of the existing scientific knowledge to develop improved DS treatments and cures. Leading authors review the state-of-the-art in their field of investigation and provide their views and perspectives for future research Chapters are extensively referenced to provide readers with a comprehensive list of resources on the topics covered All chapters include comprehensive background information and are written in a clear form that is also accessible to the non-specialist
Author: Andrea Poretti
Publisher: Springer
ISBN: 3319145681
Category : Medical
Languages : en
Pages : 175
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Book Description
This book discusses the key features of normal, age-dependent neonatal head ultrasonography as well as the findings of the most common neonatal neurological disorders as visualized by this modality. Neonatal head ultrasound is an important diagnostic tool in the initial evaluation of intracranial abnormalities in newborns. Head ultrasound is a safe and cost-efficient tool for detecting brain abnormalities in preterm and term neonates, monitoring the progression of brain lesions, and describing the maturation of the developing neonatal brain. To facilitate its use at the bedside, the book is organized by clinical findings and their differential diagnoses. For each disorder, a clinical vignette describing the clinical presentation of the newborn is accompanied by high-quality ultrasound images that depict the abnormal findings and detailed explanations of these findings. This book is a succinct guide to neonatal head ultrasonography for neuroradiologists, neonatologists, and pediatricians.
Author: H.F. Baars
Publisher: Springer Science & Business Media
ISBN: 1849964718
Category : Medical
Languages : en
Pages : 453
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Book Description
Clinical management and signs are the focus of this practical cardiogenetic reference for those who are involved in the care for cardiac patients with a genetic disease. With detailed discussion of the basic science of cardiogenetics in order to assist in the clinical understanding of the topic. The genetic causes of various cardiovascular diseases are explained in a concise clinical way that reinforces the current management doctrine in a practical manner. The authors will cover the principles of molecular genetics in general but also specific to cardiac diseases. They will discuss the etiology, pathogenesis, pathophysiology, clinical presentation, clinical diagnosis, molecular diagnosis and treatment of each cardiogenetic disease separately. Therapy advice, ICD indications, indications for and manner of further family investigation will all be covered, while each chapter will also contain take-home messages to reinforce the key points. The chapters reviewing the different diseases will each contain a table describing the genes involved in each. Each chapter will also contain specific illustrations, cumulatively giving a complete, practical review of each cardiogenetic disease separately. Special emphasis will be given to advice on how to diagnose and manage cardiogenetic diseases in clinical practice, which genes should be investigated and why, and the pros and cons of genetic testing. Guidelines for investigation in families with sudden cardiac death at young age will also be included. This book will be written for the general cardiologist and the clinical geneticist who is involved in cardiac patients and will provide answers to question such as: Which genes are involved and which mutations? What is the effect of the mutation at cellular level? Which genes should be tested and why? What is the value of a molecular diagnosis? Does it influence therapy? When should the first degree relatives be tested and in which way?
