Overview

This practical guide adopts a symptom-based approach allowing the clinician to reach a relevant differential diagnosis and give appropriate genetic counseling. It also informs as to which genetic tests are available, with emphasis on understanding the value and need for such tests. Most contemporary texts are multi-author and often lack a themed and consistent approach to the patient. The purpose of this book is not to provide an exhaustive list to all known mutations, but to guide the physician through the process of diagnosing, counseling and, if necessary, molecular genetic testing the individual with, or at risk of, a neurogenetic condition.

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9780750654104

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