Small 4p16.3 deletions: Three additional patients and review of the literature

Laura Bernardini, Francesca C Radio, Fabio Acquaviva, Cristina Gorgone, Diana Postorivo, Barbara Torres, Viola Alesi, Monia Magliozzi, Fortunato Lonardo, Matteo Della Monica, Anna M Nardone, Claudia Cesario, Teresa Mattina, Gioacchino Scarano, Bruno Dallapiccola, Maria C Digilio, Antonio Novelli

Research output: Contribution to journalArticle

Abstract

Wolf-Hirschhorn syndrome is a well-defined disorder due to 4p16.3 deletion, characterized by distinct facial features, intellectual disability, prenatal and postnatal growth retardation, and seizures. Genotype-phenotype correlations based on differently sized deletions have been attempted, and some candidate genes have been suggested. We report on clinical characteristics of three patients with pure interstitial submicroscopic 4p16.3 deletions, ranging in size from 68 to 166 kb, involving WHSCR1 and/or part of WHSCR2, and review published cases with overlapping 4p16.3 losses. The present study highlights a major role of NSD2 gene in the pathogenesis of the WHS main features and predicts that loss-of-function mutations affecting NSD2 gene could result in microcephaly, prenatal and postnatal growth retardation, psychomotor and language delay, and craniofacial features. Absent seizures in all subjects corroborate the suggestion that this specific feature is causally linked with at least one additional causative gene. Finally, we suggest that mir-943 could play a role in the pathogenesis of CHD in some of these patients.

Original languageEnglish
JournalAmerican Journal of Medical Genetics, Part A
DOIs
Publication statusE-pub ahead of print - Sep 23 2018

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Genes
Seizures
Wolf-Hirschhorn Syndrome
Language Development Disorders
Microcephaly
Genetic Association Studies
Growth
Intellectual Disability
Mutation

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Small 4p16.3 deletions : Three additional patients and review of the literature. / Bernardini, Laura; Radio, Francesca C; Acquaviva, Fabio; Gorgone, Cristina; Postorivo, Diana; Torres, Barbara; Alesi, Viola; Magliozzi, Monia; Lonardo, Fortunato; Monica, Matteo Della; Nardone, Anna M; Cesario, Claudia; Mattina, Teresa; Scarano, Gioacchino; Dallapiccola, Bruno; Digilio, Maria C; Novelli, Antonio.

In: American Journal of Medical Genetics, Part A, 23.09.2018.

Research output: Contribution to journalArticle

Bernardini, L, Radio, FC, Acquaviva, F, Gorgone, C, Postorivo, D, Torres, B, Alesi, V, Magliozzi, M, Lonardo, F, Monica, MD, Nardone, AM, Cesario, C, Mattina, T, Scarano, G, Dallapiccola, B, Digilio, MC & Novelli, A 2018, 'Small 4p16.3 deletions: Three additional patients and review of the literature', American Journal of Medical Genetics, Part A. https://doi.org/10.1002/ajmg.a.40512
Bernardini, Laura ; Radio, Francesca C ; Acquaviva, Fabio ; Gorgone, Cristina ; Postorivo, Diana ; Torres, Barbara ; Alesi, Viola ; Magliozzi, Monia ; Lonardo, Fortunato ; Monica, Matteo Della ; Nardone, Anna M ; Cesario, Claudia ; Mattina, Teresa ; Scarano, Gioacchino ; Dallapiccola, Bruno ; Digilio, Maria C ; Novelli, Antonio. / Small 4p16.3 deletions : Three additional patients and review of the literature. In: American Journal of Medical Genetics, Part A. 2018.
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