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

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