Jump to content

Kufor–Rakeb syndrome

From Wikipedia, the free encyclopedia

This is an old revision of this page, as edited by Tom.Reding (talk | contribs) at 00:29, 27 May 2016 (top: CS1 maintenance: vauthors/veditors or enumerate multiple authors/editors; WP:GenFixes on, using AWB). The present address (URL) is a permanent link to this revision, which may differ significantly from the current revision.

Kufor–Rakeb syndrome

Kufor–Rakeb syndrome is an autosomal recessive disorder.[1]

It can be associated with ATP13A2

References

  1. ^ Williams DR, Hadeed A, al-Din AS, Wreikat AL, Lees AJ (October 2005). "Kufor–Rakeb disease: autosomal recessive, levodopa-responsive parkinsonism with pyramidal degeneration, supranuclear gaze palsy, and dementia". Mov. Disord. 20 (10): 1264–71. doi:10.1002/mds.20511. PMID 15986421.