Hereditary spastic paraplegia

SYNONIMS: Strumpell-Lorrain syndrome

ICD10 code: G11.4

ORPHANET number: ORPHA685

For more information about this disease, please visit the Orphanet website.
Visitors from North America may also contact NIH Office of Rare Diseases Research website.

RARE DISEASES LIBRARY:

You may find a detailed description of Hereditary spastic paraplegia in Issue 16 of “Rare Diseases & Orphan Drugs”. Click here to open the pdf-file (file size 690 KB).

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Last modification: 10:36 27.08.2010
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