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Hum Genet ; 109(1): 1-6, 2001 Jul.
Article in English | MEDLINE | ID: mdl-11479728

ABSTRACT

Holoprosencephaly (HPE) is genetically heterogeneous with four genes, SIX3, SHH, TGIF, and ZIC2 that have been identified to date and that are altered in 12% of patients. To analyze this prevalence in a South American population-based sample (57 HPE cases in 244,511 live and still births or 1 in 4300), we performed a mutational study of these genes in 30 unrelated children (26 newborns and 4 non-newborns) with HPE being ascertained by ECLAMC (Latin American Collaborative Study of Congenital Malformations). We identified three novel mutations: two were missense mutations of the SHH gene (Cys183-->Phe; His140-->Pro); the third mutation was a 2-bp deletion in the zinc-finger region of the ZIC2 gene. These molecular results explained 8% (2/26 newborn samples) of the HPE cases in this South American population-based sample, a proportion similar to our previously published data from a collection of cases.


Subject(s)
Holoprosencephaly/genetics , Mutation , Trans-Activators/genetics , Transcription Factors/genetics , Base Sequence , DNA/genetics , DNA Mutational Analysis , Female , Fetal Death/genetics , Genetics, Population , Hedgehog Proteins , Holoprosencephaly/epidemiology , Humans , Infant , Infant, Newborn , Male , Mutation, Missense , Nuclear Proteins , Sequence Deletion , South America/epidemiology
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