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The fragile X syndrome

B D Patel1

  • 1Department of Paediatrics, Addenbrooke's Hospital, University of Cambridge.

The British Journal of Clinical Practice
|January 1, 1994
PubMed
Summary

Fragile X syndrome, the most common cause of inherited intellectual disability, is frequently underestimated. This genetic disorder places a significant long-term burden on families and healthcare services.

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Area of Science:

  • Genetics
  • Neurodevelopmental Disorders
  • Public Health

Background:

  • Fragile X syndrome is a leading genetic cause of intellectual disability.
  • Its prevalence and impact are often underestimated in clinical and research settings.
  • Understanding its role is crucial for families and healthcare systems.

Purpose of the Study:

  • To highlight the significant, yet underestimated, contribution of Fragile X syndrome to intellectual disability.
  • To emphasize its status as a common genetic disease with substantial familial and societal costs.

Main Methods:

  • This abstract does not detail specific methods.
  • The study likely involves a review or analysis of existing data on Fragile X syndrome prevalence and impact.
  • Further research may include genetic studies and epidemiological surveys.

Main Results:

  • Fragile X syndrome is the most common form of familial intellectual disability.
  • It is one of the most prevalent genetic diseases.
  • The long-term burden on families and services is considerable.

Conclusions:

  • The impact of Fragile X syndrome on intellectual disability is significantly underestimated.
  • Recognizing its prevalence and burden is essential for effective support and resource allocation.
  • Further investigation into the genetic and social aspects of Fragile X syndrome is warranted.

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