• Abbas Tafakhori, Alvin Yu Jin Ng, Sumanty Tohari, Byrappa Venkatesh, Hane Lee, Ascia Eskin, Stanley F Nelson, Carine Bonnard, Bruno Reversade, and Ariana Kariminejad.
• Iranian Center of Neurological Research, Neurology Department, Tehran University of Medical Sciences, Tehran, Iran.
• Arch Iran Med. 2016 Feb 1; 19 (2): 87-91.

BackgroundTWINKLE (c10orf2) gene is responsible for autosomal dominant progressive external ophthalmoplegia (PEO). In rare cases, additional features such as muscle weakness, peripheral neuropathy, ataxia, cardiomyopathy, dysphagia, dysphonia, cataracts, depression, dementia, parkinsonism, and hearing loss have been reported in association with heterozygous mutations of the TWINKLE gene.MethodsWe have studied a large Iranian family with myopathy, dysphonia, dysphagia, and behavior change in addition to PEO in affected members.ResultsWe identified a missense mutation c.1121G > A in the c10orf2 gene in all affected members. Early death is a novel feature seen in affected members of this family that has not been reported to date.ConclusionThe association of PEO, myopathy, dysphonia, dysphagia, behavior change and early death has not been previously reported in the literature or other patients with this mutation.

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