C5orf42 is the major gene responsible for OFD syndrome type VI View Full Text


Ontology type: schema:ScholarlyArticle     


Article Info

DATE

2014-03

AUTHORS

Estelle Lopez, Christel Thauvin-Robinet, Bruno Reversade, Nadia El Khartoufi, Louise Devisme, Muriel Holder, Hélène Ansart-Franquet, Magali Avila, Didier Lacombe, Pascale Kleinfinger, Irahara Kaori, Jun-Ichi Takanashi, Martine Le Merrer, Jelena Martinovic, Catherine Noël, Mohammad Shboul, Lena Ho, Yeliz Güven, Ferechté Razavi, Lydie Burglen, Nadège Gigot, Véronique Darmency-Stamboul, Julien Thevenon, Bernard Aral, Hülya Kayserili, Frédéric Huet, Stanislas Lyonnet, Cédric Le Caignec, Brunella Franco, Jean-Baptiste Rivière, Laurence Faivre, Tania Attié-Bitach

ABSTRACT

Oral-facial-digital syndrome type VI (OFD VI) is a recessive ciliopathy defined by two diagnostic criteria: molar tooth sign (MTS) and one or more of the following: (1) tongue hamartoma (s) and/or additional frenula and/or upper lip notch; (2) mesoaxial polydactyly of one or more hands or feet; (3) hypothalamic hamartoma. Because of the MTS, OFD VI belongs to the "Joubert syndrome related disorders". Its genetic aetiology remains largely unknown although mutations in the TMEM216 gene, responsible for Joubert (JBS2) and Meckel-Gruber (MKS2) syndromes, have been reported in two OFD VI patients. To explore the molecular cause(s) of OFD VI syndrome, we used an exome sequencing strategy in six unrelated families followed by Sanger sequencing. We identified a total of 14 novel mutations in the C5orf42 gene in 9/11 families with positive OFD VI diagnostic criteria including a severe fetal case with microphthalmia, cerebellar hypoplasia, corpus callosum agenesis, polydactyly and skeletal dysplasia. C5orf42 mutations have already been reported in Joubert syndrome confirming that OFD VI and JBS are allelic disorders, thus enhancing our knowledge of the complex, highly heterogeneous nature of ciliopathies. More... »

PAGES

367-377

References to SciGraph publications

Identifiers

URI

http://scigraph.springernature.com/pub.10.1007/s00439-013-1385-1

DOI

http://dx.doi.org/10.1007/s00439-013-1385-1

DIMENSIONS

https://app.dimensions.ai/details/publication/pub.1049964831

PUBMED

https://www.ncbi.nlm.nih.gov/pubmed/24178751


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