SPG6 HSP study

Posted - June 2011 in Research Highlights

 

Complicated HSP case identified

 

The first complicated case of SPG6 in the world has been identified in a study of 86 Chinese HSPers with SPG6.

 

 

BACKGROUND:

Hereditary spastic paraplegia type 6 (SPG6) is caused by mutations in the NIPA1 gene. This is a rare cause of HSP and until now, all the affected individuals reported displayed “pure” spastic paraplegia.

OBJECTIVES:

To analyze the genotype/phenotype correlation of mutations so far described in NIPA1.

METHODS:

Eighty-six Chinese Han HSP patients were investigated for SPG6 mutations by direct sequencing of the NIPA1 gene.

RESULTS:

One heterozygous missense mutation c.316G>C/p.G106R was identified in a complicated form of ADHSP family with peripheral nerves disease, and SPG6 mutation in our sample accounted for 3.6% (1/28) of ADHSP families and 1.1% (1/86) of non-ARHSP patients who were negative for SPG4, SPG3A and SPG31 mutations.

CONCLUSIONS:

We report the first complicated case of SPG6 in the world by the presence of peripheral neuropathy, which extends the phenotype initially described.

 

SOURCE:  Clin Neurol Neurosurg. 2011 Mar 16. [Epub ahead of print]

Expansion of the phenotypic spectrum of SPG6 caused by mutation in NIPA1.

Du J, Hu YC, Tang BS, Chen C, Luo YY, Zhan ZX, Zhao GH, Jiang H, Xia K, Shen L.

 

Department of Neurology, Xiangya Hospital, Central South University, Changsha, Hunan 410008, China.

 

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