Fragile X (FMR1)CGG Repeat Analysis

Identify Fragile X syndrome with the Fragile X (FMR1) CGG Repeat Analysis Test at Lucid Medical Diagnostics in Hyderabad. This advanced molecular genetic test measures the number of CGG repeats in the FMR1 gene to detect normal, intermediate, premutation, and full mutation alleles associated with Fragile X syndrome. The test supports the diagnosis of intellectual disability, autism spectrum disorders, developmental delay, and carrier status assessment, as well as reproductive risk evaluation. Using advanced molecular diagnostic technology and stringent quality standards, Lucid Medical Diagnostics delivers accurate, reliable, and timely results to support informed clinical decisions, genetic counseling, and personalized patient care.

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