Association of mutations in FLNA with craniosynostosis.

Abstract

Mutations of FLNA, an X-linked gene that encodes the cytoskeletal protein filamin A, cause diverse and distinct phenotypes including periventricular nodular heterotopia and otopalatodigital spectrum disorders (OPDS). Craniofacial abnormalities associated with OPDS include supraorbital hyperostosis, down-slanting palpebral fissures and micrognathia; craniosynostosis was previously described in association with FLNA mutations in two individual case reports. Here we present four further OPDS subjects who have pathological FLNA variants and craniosynostosis, supporting a causal link. Together with the previously reported patients, frontometaphyseal dysplasia was the most common clinical diagnosis (four of six cases overall); five patients had multiple suture synostosis with the sagittal suture being the most frequently involved (also five patients). No genotype-phenotype correlation was evident in the distribution of FLNA mutations. This report highlights the need to consider a filaminopathy in the differential diagnosis of craniosynostosis, especially in the presence of atypical cranial or skeletal features.

• Authors: Nathalie Fennell, Nicola Foulds, Diana S Johnson, Louise C Wilson, Michelle Wyatt, Stephen P Robertson, David Johnson, Steven A Wall, Andrew O M Wilkie
• Journal: European journal of human genetics : EJHG (Eur J Hum Genet) Vol. 23 Issue 12 Pg. 1684-8 (Dec 2015) ISSN: 1476-5438 [Electronic] England
• PMID: 25873011 (Publication Type: Case Reports, Journal Article, Research Support, Non-U.S. Gov't)

Chemical References

• FLNA protein, human
• Filamins

Topics

• Child
• Child, Preschool
• Craniosynostoses (diagnosis, genetics)
• Diagnosis, Differential
• Female
• Filamins (genetics)
• Humans
• Infant
• Male
• Mutation, Missense
• Phenotype