Fragile X syndrome risk factors

Editor-In-Chief: C. Michael Gibson, M.S., M.D. [1] Associate Editor(s)-in-Chief:

Fragile X syndrome Microchapters
Home
Patient Information
Overview
Historical Perspective
Classification
Pathophysiology
Causes
Differentiating Fragile X syndrome from other Diseases
Epidemiology and Demographics
Risk Factors
Screening
Natural History, Complications and Prognosis
Diagnosis
History and Symptoms
Physical Examination
Laboratory Findings
Other Diagnostic Studies
Treatment
Medical Therapy
Primary Prevention
Secondary Prevention
Cost-Effectiveness of Therapy
Future or Investigational Therapies
Case Studies
Case #1
Fragile X syndrome risk factors On the Web
Most recent articles
Most cited articles
Review articles
CME Programs
Powerpoint slides
Images
American Roentgen Ray Society Images of Fragile X syndrome risk factors All Images X-rays Echo & Ultrasound CT Images MRI
Ongoing Trials at Clinical Trials.gov
US National Guidelines Clearinghouse
NICE Guidance
FDA on Fragile X syndrome risk factors
CDC on Fragile X syndrome risk factors
Fragile X syndrome risk factors in the news
Blogs on Fragile X syndrome risk factors
Directions to Hospitals Treating Fragile X syndrome
Risk calculators and risk factors for Fragile X syndrome risk factors

Overview

The most potent risk factor in the development of Fragile X syndrome is presence of Fragile X syndrome in any of family members. Other risk factors include family history of developmental delays, autism or intellectual deficit of unknown origin and infertility in the family.

Risk Factors

Common risk factors in the development of Fragile X syndrome include family history of Fragile X syndrome, mental retardation or autism of unknown origin and developmental delays in the family members. Family history of infertility associated with elevated FSH levels or premature ovarian family have shown some linkage with Fragile X syndrome.