MOLECULAR AND CYTOGENETIC ANALYSIS OF THE FRAGILE-X-SYNDROME IN A SERIES OF 453 MENTALLY-RETARDED SUBJECTS - A STUDY OF 87 FAMILIES

We report on a series of 453 mentally retarded subjects investigated f or fragile X syndrome from 1982 to July 1995. The 22% rate of efficien cy of FRAX positivity indicated a significant preselection by the clin icians, However, this rate dropped to 11% in the last year. Since 1992 , Southern blot analysis was extended to include family members of the 87 positive subjects, for a total of 442 individuals examined with th e probe StB12.3. In addition to premutated (118), fully mutated (148), and pre/full mutation mosaic subjects (27), 14 atypical cases were fo und. Some of these cases are described in more detail, In particular, we report on the hybridization and polymerase chain reaction data of 2 fragile X subjects with full mutation and a 2.8-kb allele and 1 with fall mutation and a 2.4-kb allele, An intellectually normal male with 18% of fraXq27.3 and an unmethylated full mutation is also described, Finally, a mentally retarded child with only a lower allele of 2.7 kb is presented. (C) 1996 Wiley-Liss, Inc.