Literature DB >> 8533829

Recurrent lambdoid synostosis within two families.

J S Fryburg1, V Hwang, K Y Lin.   

Abstract

We report on 2 families with multiple members who have proven or suspected lambdoid craniosynostosis. In one family the lambdoid suture was unilaterally involved in one sib, and bilaterally in the other. In the second family the propositus had unilateral lambdoid synostosis and his twin sisters each had bilateral lambdoid synostosis. Both families had another distant relative, a maternal grandmother in the first and paternal uncle in the second, who were also reported to have posterior plagiocephaly. We report these families as evidence for genetic transmission of a craniosynostotic trait which has only been rarely reported previously.

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Year:  1995        PMID: 8533829     DOI: 10.1002/ajmg.1320580313

Source DB:  PubMed          Journal:  Am J Med Genet        ISSN: 0148-7299


  4 in total

Review 1.  Genetic basis of single-suture synostoses: genes, chromosomes and clinical implications.

Authors:  Wanda Lattanzi; Nenad Bukvic; Marta Barba; Gianpiero Tamburrini; Camilla Bernardini; Fabrizio Michetti; Concezio Di Rocco
Journal:  Childs Nerv Syst       Date:  2012-08-08       Impact factor: 1.475

Review 2.  Genetic advances in craniosynostosis.

Authors:  Wanda Lattanzi; Marta Barba; Lorena Di Pietro; Simeon A Boyadjiev
Journal:  Am J Med Genet A       Date:  2017-02-04       Impact factor: 2.802

3.  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

4.  Familial incidence and associated symptoms in a population of individuals with nonsyndromic craniosynostosis.

Authors:  Jaclyn Greenwood; Pamela Flodman; Kathryn Osann; Simeon A Boyadjiev; Virginia Kimonis
Journal:  Genet Med       Date:  2013-09-26       Impact factor: 8.822

  4 in total

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