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      [Turner syndrome and mosaicism].

      1
      Bulletin de l'Academie nationale de medecine

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          Abstract

          Turner's syndrome is a gonadosomatic dysgenesis of female phenotype due to a more or less complete monosomy of one of the X chromosomes leading to a haploinsufficiency of the development genes situated at the level of the pseudoautosomal region of the gonosomes. Further experience of the karyotype showed a preponderance of mosaics and considerable variability of Turner's phenotype in proportion to the number of 45, X cells. The rare cases of monozygotism discordant with variable tissular distribution mosaics show that the phenotypic expression is a genic dosage effect. In patients with TS it would thus be of interest to study a second tissue such skin fibroblasts when a discordance is observed between the phenotype and the karyotype.

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          Author and article information

          Journal
          Bull. Acad. Natl. Med.
          Bulletin de l'Academie nationale de medecine
          0001-4079
          0001-4079
          2003
          : 187
          : 2
          Affiliations
          [1 ] Service de Génétique Médicale-Hôpital des Enfants-CHU Pellegrin-Place Amélie Raba-Léon-33076 Bordeaux.
          Article
          14556446
          eaadb16e-a1b3-4722-8a55-e8dde2a7fafc
          History

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