Literature DB >> 18195151

POLG1 mutations manifesting as autosomal recessive axonal Charcot-Marie-Tooth disease.

Timothy Harrower1, Joanna D Stewart, Gavin Hudson, Henry Houlden, Graham Warner, Dominic G O'Donovan, Leslie J Findlay, Robert W Taylor, Rajith De Silva, Patrick F Chinnery.   

Abstract

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 gamma-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.

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Year:  2008        PMID: 18195151     DOI: 10.1001/archneurol.2007.4

Source DB:  PubMed          Journal:  Arch Neurol        ISSN: 0003-9942


  11 in total

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