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POLG1 Mutations Manifesting as Autosomal Recessive Axonal Charcot-Marie-Tooth Disease
Timothy Harrower, MRCP;
Joanna D. Stewart, BSc;
Gavin Hudson, PhD;
Henry Houlden, MRCP(UK);
Graham Warner, MRCP;
Dominic G. O’Donovan, FRCPath;
Leslie J. Findlay, FRCP;
Robert W. Taylor, PhD;
Rajith De Silva, FRCP;
Patrick F. Chinnery, PhD, FRCP
Arch Neurol. 2008;65(1):133-136.
Background Although a molecular diagnosis is possible in most patients having Charcot-Marie-Tooth disease (CMT), recessively inherited and axonal neuropathies still present a diagnostic challenge.
Objective To determine the cause of axonal CMT type 2 in 3 siblings.
Design Case report.
Setting Academic research.
Participants Three siblings who subsequently developed profound cerebellar ataxia.
Main Outcome Measures Muscle biopsy specimen molecular genetic analysis of the POLG1 (polymerase  -1) gene, as well as screening of control subjects for POLG1 sequence variants.
Results Cytochrome c oxidase deficient fibers and multiple deletions of mitochondrial DNA were detected in skeletal muscle. Three compound heterozygous substitutions were detected in POLG1.
Conclusion Even in the absence of classic features of mitochondrial disease, POLG1 should be considered in patients having axonal CMT that may be associated with tremor or ataxia.
Author Affiliations: Departments of Neurology (Drs Harrower, O’Donovan, Findlay, and De Silva) and Neuropathology (Dr O’Donovan), Essex Centre for Neurological Sciences, Queen's Hospital, Romford; Mitochondrial Research Group, The Medical School (Drs Hudson, Taylor, and Chinnery and Ms Stewart), and Institute of Human Genetics (Drs Taylor and Chinnery), Newcastle University, Newcastle upon Tyne; Institute of Neurology and The National Hospital for Neurology and Neurosurgery, London (Dr Houlden); and Department of Neurology, Royal Surrey County Hospital, Guildford (Dr Warner); England.
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