Fragile X Syndrome: Understanding the Causes, Diagnosis, and Treatment Options

Fragile X syndrome is a neurological developmental disorder considered the most common monogenic, inheritable cause of cognitive impairment. Mutations in the FMR1 gene can also lead to various disease patterns in adulthood. Written by Frank Hler, David Pittrow, and Michael Seidel, this comprehensive book provides an in-depth exploration of the clinical picture of affected individuals, delving into the clinical and genetic diagnosis, as well as current therapy options.

Clinical Diagnosis and Therapy Options

The book offers a detailed examination of the diagnosis and treatment of Fragile X syndrome, covering the latest research and findings in the field. Readers will gain a deeper understanding of the genetic components of the disorder and the various therapy options available to manage its symptoms.

Associated Disorders and Everyday Challenges

In addition to its in-depth coverage of Fragile X syndrome, the book also explores associated disorders and everyday challenges faced by individuals with the condition. The authors provide practical insights and advice on managing these challenges, making it an invaluable resource for healthcare professionals, families, and individuals affected by the disorder.

Published by UNI-MED Verlag AG, this German-language book is a valuable resource for anyone seeking to understand Fragile X syndrome and its implications. First published on December 23, 2015, it remains a timely and authoritative guide to this complex condition.