fragile X syndrome(redirected from Fragile X syndrome type 3)
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Related to Fragile X syndrome type 3: Down syndrome, Klinefelter syndrome, Williams syndrome, Angelman syndrome, Rett syndrome, Turner syndrome, Prader Willi syndrome
fragile X syndrome[‚fraj·əl ′eks ‚sin‚drōm]
A hereditary condition resulting from a trinucleotide repeat at an inherited fragile site on the long arm of the X chromosome. Affected males usually have some characteristic facial features, enlarged testes, and mental retardation. Females with on fragile X chromosome and one normal X chromosome may have a lesser degree of mental retardation.
McGraw-Hill Dictionary of Scientific & Technical Terms, 6E, Copyright © 2003 by The McGraw-Hill Companies, Inc.