Literature DB >> 10215540

Craniosynostosis associated with ectopia lentis in monozygotic twin sisters.

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.

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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


  2 in total

1.  Lambdoidal synostosis in dizygotic twins with a family history of an undiagnosed connective tissue disorder.

Authors:  Caroline C Watson; Christoph J Griessenauer; R Shane Tubbs; James M Johnston
Journal:  Childs Nerv Syst       Date:  2013-11-06       Impact factor: 1.475

2.  Mechanism of Disease: Recessive ADAMTSL4 Mutations and Craniosynostosis with Ectopia Lentis.

Authors:  Jonas Gustafson; Maria Bjork; Conny M A van Ravenswaaij-Arts; Michael L Cunningham
Journal:  Case Rep Genet       Date:  2022-03-26
  2 in total

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