Literature DB >> 265609

Variable expressivity of Crouzon's syndrome within a family.

S Kreiborg, B L Jensen.   

Abstract

Three individuals in two generations affected with Crouzon's syndrome are reported. The proband, a 10-year-old boy, had been diagnosed until the age of 4. His 3-year-old sister had not been diagnosed previously and his mother was unaware of having the syndrome and had never received any genetic counseling. The individuals are reported with emphasis on clinical and roentgencephalometric variation. The ultimate goal in teratolgoy is prevention. Currently one of the most important factors related to prevention is genetic counseling in conditions with well-documented modes of inheritance. The present report describes how the variable expressivity of Crouzon's syndrome within a family had caused diagnostic problems and consequently had delayed genetic counseling.

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Year:  1977        PMID: 265609     DOI: 10.1111/j.1600-0722.1977.tb00551.x

Source DB:  PubMed          Journal:  Scand J Dent Res        ISSN: 0029-845X


  2 in total

1.  Germinal mosaicism in Crouzon syndrome.

Authors:  S Kreiborg; M M Cohen
Journal:  Hum Genet       Date:  1990-04       Impact factor: 4.132

2.  Crouzon syndrome is not linked to craniosynostosis loci at 7p and 5qter.

Authors:  W Reardon; L van Herwerden; C Rose; B Jones; S Malcolm; R M Winter
Journal:  J Med Genet       Date:  1994-03       Impact factor: 6.318

  2 in total

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