Genetic Counseling for Adult Neurogenetic Disease -

Genetic Counseling for Adult Neurogenetic Disease

A Casebook for Clinicians

Jill S. Goldman (Herausgeber)

Buch | Softcover
325 Seiten
2017 | Softcover reprint of the original 1st ed. 2015
Springer-Verlag New York Inc.
978-1-4899-7837-0 (ISBN)
64,19 inkl. MwSt
The adult patient diagnosed with or at risk for a neurogenetic disease has many questions and concerns for the genetic counselor, the neurologist, and other practitioners. Because of the emotional and potentially life-altering impact of these diseases on the patient and family, counseling can be especially challenging.

A rare hands-on guide to the subject, Genetic Counseling for Adult Neurogenetic Disease deals with core issues that differentiate adult neurogenetic counseling from its more familiar pediatric counterpart. This innovative book with accompanying videos is designed to fill in deficits in this area typical of training programs in genetic counseling (which have pediatrics and prenatal concentrations) and neurology (which rarely cover genetic counseling). For each condition featured, chapters include a detailed overview of genetic symptoms, diagnostic criteria, and management, plus guidelines for asking, and answering, pertinent questions. The major concentration, however, is on genetic counseling issues and case histories illustrating these issues. As an added dimension, the accompanying videos depict representative issues and challenges in genetic counseling for specific diseases in addition to the basics of a neurological examination. Among the conditions discussed:



Movement disorders, including Parkinson's disease.
Dementias, including Alzheimer's disease.
Stroke.
Motor neuron diseases.
Neuropathies and channelopathies.
Adult muscular dystrophies.
Neurocutaneous syndromes.
Plus a section on neurological and neuropsychological evaluation.

This is information that will stay relevant as technologies change and genetic understanding evolves. Genetic Counseling for Adult Neurogenetic Disease offers advanced clinical wisdom for genetic counselors as well as neurologists, neuropsychologists, and other referring clinicians.

Jill Goldman has been a neurogenetic counselor for 12 years at UCSF and Columbia University. She has first authored many papers including the 2011 “Genetic counseling and testing for Alzheimer disease: Joint practice guidelines of the American College of Medical Genetics and the National Society of Genetic Counselors” published in Genetics in Medicine. Jill is Chairperson of the Education Committee of the Medical Advisory Committee of the Association for Frontotemporal Degeneration. She has extensive experience in educating health professionals on neurogenetic diseases including teaching genetic counseling students, genetic counselors, genetics residents and fellows, nursing students, medical trainees, and the lay public. She has organized a NYC Frontotemporal Dementia Caregiver Conference and a Columbia University CME course for psychiatrists and neurologists on Alzheimer’s disease and Frontotemporal Degeneration. Jill was co-chair of a 2001 NSGC Annual Educational Conference workshop on neurogenetics and the 2004 Short Course on Neurogenetics. She has supervised both prospective and active genetic counseling students. Jill has also been a co-chair for the NSGC Neurogenetics SIG and a member of the Ethics Committee and Abstracts Committee. In addition to being Project Director, she will be responsible for sections on dementia and movement disorders.

Part 1:The Movement Disorders.- 1.Overview.- 2.Huntington Disease.- 3.Parkinson Disease.- 4.Dystonia.- 5.Ataxia.- Part 2:The Dementias.- 6.Overview.- 7.Alzheimer’s Disease.- 8.Frontotemporal Degeneration.- 9.Prion Diseases.- Part 3:Stroke.- 10.Overview of Cerebrovascular Disease and Stroke Risk Factors.- 11.CADASIL.- Part 4:The Motor Neuron Diseases.- 12.Overview.- 13.Amyotrophic Lateral Sclerosis.- 14.Spinal Bulbar Muscular Atrophy: Kennedy’s Disease.- 15.Hereditary Spastic Paraplegia.- Part 5:The Neuropathies and Channelopathies.- 16.Charcot Marie Tooth.- 17.Channelopathies.- 18.Overview.- 19.The Myopathies.- 20.The Muscular Dystrophies.- 21.The Myotonic Dystrophies.- Part 7:Neurocutaneous Syndromes.- 22.Overview.- 23.Neurofibromatosis.- 24.Tuberous sclerosis.- Part 8:The Clinical Evaluation.- 25.The Neurological Examination and Testing.- 26.The Neuropsychological Evaluation.

Erscheinungsdatum
Zusatzinfo 20 Illustrations, black and white; XIX, 325 p. 20 illus.
Verlagsort New York
Sprache englisch
Maße 155 x 235 mm
Themenwelt Geisteswissenschaften Psychologie Sozialpsychologie
Medizin / Pharmazie Gesundheitswesen
Medizin / Pharmazie Medizinische Fachgebiete Psychiatrie / Psychotherapie
Studium 2. Studienabschnitt (Klinik) Humangenetik
Sozialwissenschaften Soziologie
Schlagworte adult neurogenetic disease • Creutzfeld-Jacob disease • family genetic counseling • genetic counseling for neurogenetic cases • inherited diseases • progressive supranuclear palsy
ISBN-10 1-4899-7837-2 / 1489978372
ISBN-13 978-1-4899-7837-0 / 9781489978370
Zustand Neuware
Haben Sie eine Frage zum Produkt?
Mehr entdecken
aus dem Bereich
Eine sehr persönliche Geschichte | Der New York Times-Bestseller

von Siddhartha Mukherjee

Buch | Softcover (2023)
Ullstein Taschenbuch Verlag
21,99
Die revolutionäre Medizin von morgen (Lifespan)

von David A. Sinclair; Matthew D. LaPlante

Buch | Softcover (2020)
DuMont Buchverlag
16,00