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Family History and Clefting as Major Criteria for CHARGE Syndrome
Journal article   Open access   Peer reviewed

Family History and Clefting as Major Criteria for CHARGE Syndrome

Susan Starling Hughes, Holly I. Welsh, Nicole P. Safina, Khemissa Bejaoui and Holly H. Ardinger
American journal of medical genetics. Part A, Vol.164(1), pp.48-53
01/01/2014
DOI: 10.1002/ajmg.a.36192
PMID: 24214489
url
https://doi.org/10.1002/ajmg.a.36192View
Published (Version of record) Open Access

Abstract

CHARGE syndrome is an autosomal dominant malformation syndrome associated with mutations in CHD7. The condition is typically sporadic with few familial cases reported. The diagnosis of CHARGE syndrome is based on a combination of major and minor criteria comprised of structural and functional abnormalities, most of which are part of the original CHARGE acronym, although additional anomalies have been added. To date, family history has not been considered in the diagnostic criteria. Here we report a family with a previously unreported missense mutation in exon 31 of CHD7, in which family history played a role in the diagnosis of CHARGE syndrome. Given the tremendous phenotypic variability and the dominant nature of CHARGE syndrome, we propose that family history be included as a major diagnostic criterion. A positive family history would include any individual with an apparently isolated unilateral major CHARGE anomaly or someone with a few of the minor features. Our cases support this proposal; had family history not been considered in this case, CHD7 testing might not have been pursued, leading to incomplete medical follow-up and erroneous genetic counseling. Additionally, with the increased incidence of orofacial clefting in this family, as well as in the literature, we suggest that cleft lip and/or palate be added to the major diagnostic criteria for CHARGE syndrome. (c) 2013 Wiley Periodicals, Inc.
 Genetics & Heredity Life Sciences & Biomedicine Science & Technology

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