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This book should serve as a resource for professionals in all
fields regarding diagnosis, management, and counseling of patients
with FXTAS, FXPOI and their families, as well as presenting the
molecular basis for disease that may lead to the identification of
new markers to predict disease risk and eventually lead to target
treatments. The book will present information on all aspects of
FXTAS, FXPOI and other premutation disorders including clinical
features and current supportive management, radiological,
psychological, and pathological findings, genotype-phenotype
relationships, animal models and basic molecular mechanisms.
Genetic counseling issues are also discussed.
This book should serve as a resource for professionals in all
fields regarding diagnosis, management, and counseling of patients
with FXTAS, FXPOI and their families, as well as presenting the
molecular basis for disease that may lead to the identification of
new markers to predict disease risk and eventually lead to target
treatments. The book will present information on all aspects of
FXTAS, FXPOI and other premutation disorders including clinical
features and current supportive management, radiological,
psychological, and pathological findings, genotype-phenotype
relationships, animal models and basic molecular mechanisms.
Genetic counseling issues are also discussed.
In Fragile X-Associated Tremor Ataxia Syndrome (FXTAS), the editors
present information on all aspects of FXTAS, including clinical
features and current supportive management, radiological,
psychological, and pathological findings, genotype-phenotype
relationships, animal models and basic molecular mechanisms.
Genetic counseling issues are also discussed. The book should serve
as a resource for professionals in all fields regarding diagnosis,
management, and counseling of patients with FXTAS and their
families, as well as presenting the molecular basis for disease
that may lead to the identification of new markers to predict
disease risk and eventually lead to target treatments.
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