Corpus ID: 6645250

Iridogoniodysgenesis syndrome: a case report.

@article{Kneevi2008IridogoniodysgenesisSA,
  title={Iridogoniodysgenesis syndrome: a case report.},
  author={T. Kne{\vz}evi{\'c} and Katja Novak-Lau{\vs} and Jelena {\vS}kunca and Z. Mandi{\'c}},
  journal={Acta clinica Croatica},
  year={2008},
  volume={47 3},
  pages={
          161-4
        }
}
  • T. Knežević, Katja Novak-Lauš, +1 author Z. Mandić
  • Published 2008
  • Medicine
  • Acta clinica Croatica
  • A rare case is presented of iridogoniodysgenesis syndrome, an autosomal dominant inheritance disorder that includes abnormalities in the differentiation of the anterior segment structures and increased values of intraocular pressure, which at long run increases the risk of glaucomatous optic neuropathy. The syndrome is diagnosed when ocular changes are accompanied by extraocular structure anomalies such as maxillary hypoplasia, micro- and anodontia, redundant periumbilical skin, inguinal hernia… CONTINUE READING

    References

    SHOWING 1-10 OF 14 REFERENCES
    Prognosis of goniotomy in primary infantile glaucoma (trabeculodysgenesis).
    • R. Shaffer
    • Medicine
    • Transactions of the American Ophthalmological Society
    • 1982
    • 72
    Autosomal dominant iridogoniodysgenesis anomaly maps to 6p25.
    • 71
    Trabeculotomy in congenital glaucoma
    • 46
    Familial hypoplasia of the iris stroma associated with glaucoma.
    • 49
    • PDF
    An analysis of treatment of congenital glaucoma by goniotomy.
    • 82
    Acta Clin Croat
    • Acta Clin Croat
    • 2008