[Incontinentia pigmenti. Study of 3 families].

@article{GarcaBravo1986IncontinentiaPS,
  title={[Incontinentia pigmenti. Study of 3 families].},
  author={Bego{\~n}a Garc{\'i}a-Bravo and Antonio Rodr{\'i}guez-Pichardo and Francisco Miguel Camacho-Mart{\'i}nez},
  journal={Annales de dermatologie et de venereologie},
  year={1986},
  volume={113 4},
  pages={301-8}
}
Ten cases of incontinentia pigmenti are reported. All patients, corresponding to three families, were female. In one case a Turner's syndrome phenotype (XO) with mosaicism 46 XX/46 X; i (Xq) was observed. This finding seems to confirm that the disease is transmitted through a dominant gene carried on the X chromosome. Dental alterations were the most frequent of associated abnormalities, being present in all 10 patients. We regard these abnormalities as important as they permit a retrospective… CONTINUE READING

From This Paper

Topics from this paper.

Citations

Publications citing this paper.

Similar Papers

Loading similar papers…