Inv(X)(p21.1;q22.1) in a man with mental retardation, short stature, general muscle wasting, and facial dysmorphism: clinical study and mutation analysis of the NXF5 gene - Archive ouverte HAL
Journal Articles American Journal of Medical Genetics Part A Year : 2003

Inv(X)(p21.1;q22.1) in a man with mental retardation, short stature, general muscle wasting, and facial dysmorphism: clinical study and mutation analysis of the NXF5 gene

Suzanna G. M. Frints
  • Function : Author
Lin Jun
  • Function : Author
Jean-Pierre Fryns
  • Function : Author
Koen Devriendt
  • Function : Author
Rudi Teulingkx
  • Function : Author
Lut van den Berghe
  • Function : Author
Bernice de Vos
  • Function : Author
Martine Borghgraef
  • Function : Author
Jamel Chelly
  • Function : Author
  • PersonId : 1054990
Vincent Des Portes
  • Function : Author
Hans van Bokhoven
  • Function : Author
Ben Hamel
  • Function : Author
Hans-Hilger Ropers
  • Function : Author
Vera Kalscheuer
  • Function : Author
Martine Raynaud
Claude Moraine
  • Function : Author
Peter Marynen
  • Function : Author
Guy Froyen
  • Function : Author

Abstract

We describe a 59-year-old male (patient A059) with moderate to severe mental retardation (MR) and a pericentric inversion of the X-chromosome: inv(X)(p21.1;q22.1). He had short stature, pectus excavatum, general muscle wasting, and facial dysmorphism. Until now, no other patients with similar clinical features have been described in the literature. Molecular analysis of both breakpoints led to the identification of a novel "Nuclear RNA export factor" (NXF) gene cluster on Xq22.1. Within this cluster, the NXF5 gene was interrupted with subsequent loss of gene expression. Hence, mutation analysis of the NXF5 and its neighboring homologue, the NXF2 gene was performed in 45 men with various forms of syndromic X-linked MR (XLMR) and in 70 patients with nonspecific XLMR. In the NXF5 gene four nucleotide changes: one intronic, two silent, and one missense (K23E), were identified. In the NXF2 gene two changes (one intronic and one silent) were found. Although none of these changes were causative mutations, we propose that NXF5 is a good candidate gene for this syndromic form of XLMR, given the suspected role of NXF proteins is within mRNA export/transport in neurons. Therefore, mutation screening of the NXF gene family in phenotypically identical patients is recommended.

Dates and versions

hal-04146361 , version 1 (29-06-2023)

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Suzanna G. M. Frints, Lin Jun, Jean-Pierre Fryns, Koen Devriendt, Rudi Teulingkx, et al.. Inv(X)(p21.1;q22.1) in a man with mental retardation, short stature, general muscle wasting, and facial dysmorphism: clinical study and mutation analysis of the NXF5 gene. American Journal of Medical Genetics Part A, 2003, 119A (3), pp.367-374. ⟨10.1002/ajmg.a.20195⟩. ⟨hal-04146361⟩
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