Delineation of a Novel Mirror Syndrome: NFIC Variants Cause Syndromic Intellectual Disability With Macrocephaly

Clinical Genetics · Published 2026-07-24 · DOI 10.1111/cge.70215

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Authors (40)

Nathalie Vanden Eynde, Lucas Hérissant, Emilie Landais, Matthieu Egloff, Marlène Rio, Geneviève Baujat, Fabienne Giuliano, Houda Karmous‐Benailly, Charles Coutton, Véronique Satre, Gaëlle Vieville, Paul Kuentz, Mathilde Nizon, Claire Beneteau, Bertrand Isidor, Patrick Callier, Valentine Marquet, Eric Bieth, Jonathan Levy, Anne‐Claude Tabet, François Cartault, Sophie Scheidecker, Aurélie Gouronc, Audrey Schalk, Chloé Angélini, Perrine Pennamen, Caroline Rooryck, Slavica Trajkova, Biljana Gagachovska, Brynn Shrom‐Model, Stephen R. Braddock, Paul Hillman, Lingying Liu, Christina Dühring Fenger, Trine Bjørg Hammer, Ina Schanze, Martin Zenker, Martine Doco‐Fenzy, Céline Poirsier, Guillaume Jouret

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Publication details

Year

2026

Citation

Eynde, N., Hérissant, L., Landais, E., et al. (2026). Delineation of a Novel Mirror Syndrome: NFIC Variants Cause Syndromic Intellectual Disability With Macrocephaly. Clinical Genetics. https://doi.org/10.1111/cge.70215

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