Register for email alerts and news feeds:
This journal | BMJ Group
rss
Published Online First: 18 November 2005. doi:10.1136/jmg.2005.038505
Journal of Medical Genetics 2006;43:541-544
Copyright © 2006 by the BMJ Publishing Group Ltd.

LETTER TO JMG

A filamin A splice mutation resulting in a syndrome of facial dysmorphism, periventricular nodular heterotopia, and severe constipation reminiscent of cerebro-fronto-facial syndrome

U Hehr1, A Hehr1, G Uyanik2, E Phelan3, J Winkler2, W Reardon3

1 Center for Human Genetics, Regensburg, Germany
2 Department of Neurology, University of Regensburg, Germany
3 Our Lady’s Hospital for Sick Children, Crumlin, Dublin 12, Ireland

Correspondence to:
Dr Ute Hehr
Center for Human Genetics, am Universitätsklinikum, D3, Franz-Josef-Strauss-Allee II, 93053 Regensburg, Germany; ute.hehr{at}humangenetik-regensburg.de

Background: Mutations of the filamin A locus (FLNA) on Xq28 have been established in girls with periventricular nodular heterotopia and in patients with otopalatodigital and overlapping phenotypes, the pathogenesis of these phenotypes being thought to be quite distinct. To date only six male cases of periventricular nodular heterotopia (PVNH) have been reported and these almost invariably associated with severe neurological signs.

Methods and Results: We report a new phenotype of male PVNH, with relatively normal development, no epilepsy or other neurological abnormality, severe constipation, and facial dysmorphism and without a discernible skeletal phenotype. This phenotype is associated with a splice site mutation in FLNA c.1923C>T, resulting in the generation of both normal and aberrant mRNA.

Conclusions: We postulate that the patient retains enough FLNA function to avoid the usual lethality associated with loss of function mutations in males and suggest that the severe constipation may be a clue to the molecular aetiology of other X linked conditions associated with severe constipation.

Abbreviations: FLNA, filamin A gene; FMD, frontometaphyseal dysplasia; MNS, Melnick-Needles syndrome; OPD1, otopalatodigital syndrome type 1; OPD2, otopalatodigital syndrome type 2; PVNH, periventricular nodular heterotopia

Keywords: cerebro-fronto-facial syndrome; constipation; filamin A; Hirschsprung disease; periventricular nodular heterotopia


Add to CiteULike CiteULike   Add to Complore Complore   Add to Connotea Connotea   Add to Del.icio.us Del.icio.us   Add to Digg Digg   Add to Reddit Reddit   Add to Technorati Technorati    What's this?

This article has been cited by other articles:

  • Sole, G, Coupry, I, Rooryck, C, Guerineau, E, Martins, F, Deves, S, Hubert, C, Souakri, N, Boute, O, Marchal, C, Faivre, L, Landre, E, Debruxelles, S, Dieux-Coeslier, A, Boulay, C, Chassagnon, S, Michel, V, Routon, M-C, Toutain, A, Philip, N, Lacombe, D, Villard, L, Arveiler, B, Goizet, C (2009). Bilateral periventricular nodular heterotopia in France: frequency of mutations in FLNA, phenotypic heterogeneity and spectrum of mutations. J. Neurol. Neurosurg. Psychiatry 80: 1394-1398 [Abstract] [Full Text]  
  • Cardoso, C., Boys, A., Parrini, E., Mignon-Ravix, C., McMahon, J. M., Khantane, S., Bertini, E., Pallesi, E., Missirian, C., Zuffardi, O., Novara, F., Villard, L., Giglio, S., Chabrol, B., Slater, H. R., Moncla, A., Scheffer, I. E., Guerrini, R. (2009). Periventricular heterotopia, mental retardation, and epilepsy associated with 5q14.3-q15 deletion. Neurology 72: 784-792 [Abstract] [Full Text]  
  • Hart, A. W., Morgan, J. E., Schneider, J., West, K., McKie, L., Bhattacharya, S., Jackson, I. J., Cross, S. H. (2006). Cardiac malformations and midline skeletal defects in mice lacking filamin A. Hum Mol Genet 15: 2457-2467 [Abstract] [Full Text]  

This Article

Services
Citing Articles
Google Scholar
PubMed
Topic Collections
Bookmark with

Register for free content

The full back archive is now available for all BMJ Journals. Institutional subscribers may access the entire archive as part of their subscription. Personal subscribers will also have access to all content when logged in. Non-subscribers who register have free access to all articles published before 2006 right back to volume 1 issue 1. Register here to access the free archive of all BMJ Journals.

Don't forget to sign up for content alerts so you keep up to date with all the articles as they are published.

Genetics jobs

Genetics jobs