Literature DB >> 17272211

Familial premature ovarian failure in female premutated carriers of fragile X syndrome: a case report and literature review.

Yu-Shiou Lin1, Man-Li Yang.   

Abstract

OBJECTIVE: The fragile X syndrome is the most common form of familial mental retardation. Most males with the FMR1 full mutation function in the mentally retarded range of intelligence. In contrast, females with the FMR1 full mutation show a broader range of intelligence. The most impressive somatic involvement that is consistently found among only premutated carrier females, not full-mutation carriers, is premature ovarian failure (POF). CASE REPORT: We report a family of fragile X syndrome. All six daughters had POF and both of the grandsons born to the daughters showed mental retardation.
CONCLUSION: We concluded that there was an association between fragile X syndrome premutation and POF, and established a model mechanism to explain the relationship.

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Year:  2006        PMID: 17272211     DOI: 10.1016/S1028-4559(09)60193-5

Source DB:  PubMed          Journal:  Taiwan J Obstet Gynecol        ISSN: 1028-4559            Impact factor:   1.705


  3 in total

Review 1.  Unstable mutations in the FMR1 gene and the phenotypes.

Authors:  Danuta Loesch; Randi Hagerman
Journal:  Adv Exp Med Biol       Date:  2012       Impact factor: 2.622

2.  Top-down or bottom-up: Contrasting perspectives on psychiatric diagnoses.

Authors:  Willem Ma Verhoeven; Siegfried Tuinier; Ineke van der Burgt
Journal:  Biologics       Date:  2008-09

Review 3.  Premature ovarian failure: a critical condition in the reproductive potential with various genetic causes.

Authors:  Farkhondeh Pouresmaeili; Zahra Fazeli
Journal:  Int J Fertil Steril       Date:  2014-03-09
  3 in total

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