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Novel POLG mutations in progressive external ophthalmoplegia mimicking mitochondrial neurogastrointestinal encephalomyopathy.

Authors: Van Goethem, G  Schwartz, M  Lofgren, A  Dermaut, B  Van Broeckhoven, C  Vissing, J 
Citation: Van Goethem G, etal., Eur J Hum Genet. 2003 Jul;11(7):547-9.
Pubmed: (View Article at PubMed) PMID:12825077
DOI: Full-text: DOI:10.1038/sj.ejhg.5201002

Autosomal recessive progressive external ophthalmoplegia (PEO) is one clinical disorder associated with multiple mitochondrial DNA deletions and can be caused by missense mutations in POLG, the gene encoding the mitochondrial DNA polymerase gamma. Mitochondrial neurogastrointestinal encephalomyopathy (MNGIE) is another autosomal recessive disorder associated with PEO and multiple deletions of mitochondrial DNA in skeletal muscle. In several patients this disorder is caused by loss of function mutations in the gene encoding thymidine phosphorylase (TP). We report a recessive family with features of MNGIE but no leukoencephalopathy in which two patients carry three missense mutations in POLG, of which two are novel mutations (N846S and P587L). The third mutation was previously reported as a recessive POLG mutation (T251I). This finding indicates the need for POLG sequencing in patients with features of MNGIE without TP mutations.


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CRRD Object Information
CRRD ID: 8694177
Created: 2014-07-28
Species: All species
Last Modified: 2014-07-28
Status: ACTIVE


RGD is funded by grant HL64541 from the National Heart, Lung, and Blood Institute on behalf of the NIH.