Literature DB >> 1605206

New York State screening program for fragile X syndrome: a progress report.

S L Nolin1, D A Snider, E C Jenkins, C S Dobkin, K Patchell, M Krawczun, G Strong, M Colwell, A Victor, T Payyapilli.   

Abstract

New York State has established a program to screen post-pubertal mentally retarded males for the fragile X [fra(X)] syndrome. The goal of the program is to identify affected males and inform their families of the diagnosis. Females in these families who are at risk for inheriting the mutation will then be able to determine their carrier status and consider that information in making reproductive decisions. Males were evaluated for 10 features of the syndrome by physicians and nurses throughout the state; cytogenetic analysis was carried out on a subset of this population. A total of 1332 males has been screened and chromosome studies have been completed for 489. Forty-three (9%) were positive for fra(X), and an additional 11 other chromosome abnormalities were identified. The 43 patients belonged to 38 families. Of the 24 families who were informed of the diagnosis, 12 consulted genetic counseling centers for follow-up studies and 12 did not.

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Year:  1992        PMID: 1605206     DOI: 10.1002/ajmg.1320430150

Source DB:  PubMed          Journal:  Am J Med Genet        ISSN: 0148-7299


  2 in total

1.  DNA testing for fragile X syndrome in schools for learning difficulties.

Authors:  S F Slaney; A O Wilkie; M C Hirst; R Charlton; M McKinley; J Pointon; Z Christodoulou; S M Huson; K E Davies
Journal:  Arch Dis Child       Date:  1995-01       Impact factor: 3.791

Review 2.  Blood specimens from patients referred for cytogenetic analysis: Vanderbilt University experience from 1985 to 1992.

Authors:  M G Butler; T Hamill
Journal:  South Med J       Date:  1995-03       Impact factor: 0.954

  2 in total

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