13
views
0
recommends
+1 Recommend
0 collections
    0
    shares
      • Record: found
      • Abstract: found
      • Article: not found

      The first detection of complete androgen insensitivity with no mutation in the coding sequence of the androgen receptor gene.

      Frontiers in bioscience : a journal and virtual library
      Adolescent, Androgen-Insensitivity Syndrome, genetics, pathology, Blotting, Northern, Cells, Cultured, DNA Mutational Analysis, DNA, Complementary, chemistry, Humans, Karyotyping, Male, Mutation, RNA, Messenger, metabolism, Receptors, Androgen, Siblings

      Read this article at

      ScienceOpenPubMed
      Bookmark
          There is no author summary for this article yet. Authors can add summaries to their articles on ScienceOpen to make them more accessible to a non-specialist audience.

          Abstract

          We have analyzed the entire nucleotide sequences of complementary DNAs of the androgen receptor gene in two siblings (patients 8044 and 8047) with complete androgen insensitivity. Plasma testosterone was in the normal male range, however, androgen binding capacity was undetectable as measured in skin fibroblasts in both patients. 5alpha-reductase activity was normal in both cases confirming that this enzyme is not involved in the mechanism of androgen insensitivity. Northern blot analysis indicated that mRNA of the AR was normal in size. In addition, no mutation was found in the entire nucleotide sequences of complementary DNAs of the androgen receptor gene. Together, our results reveal an unusual insight into the molecular basis of androgen resistance, and the molecular heterogeneity in this clinical spectrum.

          Related collections

          Author and article information

          Comments

          Comment on this article