Browse by author
Lookup NU author(s): Dr Hadil Alrohaif,
Dr Oksana Pogoryelova,
Professor Hanns Lochmuller
Full text for this publication is not currently held within this repository. Alternative links are provided below where available.
© 2018 Wiley Periodicals, Inc. Introduction: GNE myopathy is a rare recessive myopathy caused by mutations in the GNE gene. It is mainly a distal myopathy with relative sparing of the quadriceps muscle. Methods: Patients with distal myopathies from Kuwait were examined and tested for the Middle Eastern GNE gene founder mutation, p.M743T. Patients were further studied for disease-associated features. Results: GNE myopathy was confirmed in 14 of the 37 patients (37.8%) screened. All cases were caused by the p.M743T mutation. Age of onset and time from disease onset to loss of ambulation were variable. Both wasted and hypertrophied calf muscles were noted. Severely affected quadriceps were present in 1 patient, and ptosis, ophthalmoplegia, and tongue wasting in another. Discussion: The scope of the p.M743T mutation now includes the Arabian Peninsula. Variations in age of onset, disease progression, and distribution in patients harboring the same mutation suggest the role of other genetic- and environment-modifying factors. Muscle Nerve, 2018.
Author(s): Alrohaif H, Pogoryelova O, Al-Ajmi A, Aljeryan LA, Alrashidi NH, Alefasi SA, Urtizberea A, Lochmuller H, Bastaki L
Publication type: Article
Publication status: Published
Journal: Muscle and Nerve
Print publication date: 01/11/2018
Online publication date: 07/09/2018
Acceptance date: 01/09/2018
ISSN (print): 0148-639X
ISSN (electronic): 1097-4598
Publisher: John Wiley and Sons Inc.
Altmetrics provided by Altmetric