| Literature DB >> 10215540 |
J R Cruysberg1, C M van Ravenswaaij-Arts, A Pinckers, R Roddi, H G Brunner.
Abstract
Ectopia lentis has rarely been reported to occur in association with craniosynostosis, and this was found only in sporadic cases. We report on twin sisters who underwent surgery for craniosynostosis and later on, at age 3 years, were found to have bilateral ectopia lentis. Molecular studies yielded a probability of monozygosity of more than 0.98. Inheritance of the syndrome may be autosomal dominant, possibly due to a new mutation, autosomal recessive, or X-linked with male lethality.Entities:
Mesh:
Year: 1999 PMID: 10215540 DOI: 10.1002/(sici)1096-8628(19990129)82:3<201::aid-ajmg1>3.0.co;2-e
Source DB: PubMed Journal: Am J Med Genet ISSN: 0148-7299