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    Cytogenet Cell Genet. 2000;91(1-4):138-40.

    An unusual FGFR1 mutation (fibroblast growth factor receptor 1 mutation) in a girl with non-syndromic trigonocephaly.

    Kress W, Petersen B, Collmann H, Grimm T.

    Department of Human Genetics, University of Würzburg, Würzburg , Germany. wkress@biozentrum.uni-wuerzburg.de

    Non-syndromic trigonocephaly is a heterogeneous entity; in most cases the origin is unknown. Rare cases with autosomal dominant and recessive inheritance exist. Here the mutational screening of ten patients in the FGFR1, 2, and 3 genes and the TWIST gene causative of autosomal dominant craniosynostosis syndromes was reported. In one girl an unusual FGFR1 mutation was found. Copyright 2001 S. Karger AG, Basel.

    PMID: 11173846 [PubMed - indexed for MEDLINE]

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