Literature DB >> 2937295

The prenatal detection of the fragile X chromosome: review of recent experience.

E C Jenkins, W T Brown, M G Wilson, M S Lin, O S Alfi, E R Wassman, J Brooks, C J Duncan, A Masia, M S Krawczun.   

Abstract

The fragile X chromosome has been identified in specimens from 17 male and 10 female fetuses in 11 laboratories throughout the world, obtained from at least 79 fetuses at increased risk for the fra(X) syndrome. Of these, 19 were confirmed, 6 were pending, 1 was negative and 1 could not be confirmed. Twenty-five of the 79 cases were studied in our laboratory (Institute for Basic Research [IBR]) and resulted in fra(X) demonstration in specimens from 3 male and 5 female fetuses. All 3 males and 2 of the 5 females have been confirmed. When amniocytes from the two confirmed female fetuses were exposed to FUdR after culturing in Chang medium, fra(X) frequencies were virtually negative indicating that Chang medium should not be used in fragile X studies at least when FUdR is used to induce fragility. Finally, amniocytes from a fra(X) male fetus studied in 3 different laboratories exhibited strikingly different frequencies. To date, we have experienced no false-positives or negatives, but the latter case was controversial. It is recommended that laboratories undertaking fra(X) prenatal detection use a combination of at least two different proven induction systems as well as complementary DNA marker studies to prevent false negative diagnosis.

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Year:  1986        PMID: 2937295     DOI: 10.1002/ajmg.1320230123

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


  6 in total

1.  Indications for cytogenetic studies.

Authors:  Q H Qazi
Journal:  Indian J Pediatr       Date:  1989 Jul-Aug       Impact factor: 1.967

2.  Dissociation between mental retardation and fragile site expression in a family with fragile X-linked mental retardation.

Authors:  M A Voelckel; M G Mattei; C N'Guyen; N Philip; F Birg; J F Mattei
Journal:  Hum Genet       Date:  1988-12       Impact factor: 4.132

3.  Genetic mapping of the Xq27-q28 region: new RFLP markers useful for diagnostic applications in fragile-X and hemophilia-B families.

Authors:  B Arveiler; I Oberlé; A Vincent; M H Hofker; P L Pearson; J L Mandel
Journal:  Am J Hum Genet       Date:  1988-02       Impact factor: 11.025

4.  A common fragile site at Xq27: theoretical and practical implications.

Authors:  S A Ledbetter; D H Ledbetter
Journal:  Am J Hum Genet       Date:  1988-05       Impact factor: 11.025

5.  Further evidence for genetic heterogeneity in the fragile X syndrome.

Authors:  W T Brown; E C Jenkins; A C Gross; C B Chan; M S Krawczun; C J Duncan; S L Sklower; G S Fisch
Journal:  Hum Genet       Date:  1987-04       Impact factor: 4.132

6.  Multipoint genetic mapping of the Xq26-q28 region in families with fragile X mental retardation and in normal families reveals tight linkage of markers in q26-q27.

Authors:  I Oberlé; G Camerino; K Wrogemann; B Arveiler; A Hanauer; E Raimondi; J L Mandel
Journal:  Hum Genet       Date:  1987-09       Impact factor: 4.132

  6 in total

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