Kufor–Rakeb syndrome

Kufor–Rakeb syndrome is an autosomal recessive disorder of juvenile onset also known as Parkinson disease-9 (PARK9)[1].

Kufor–Rakeb syndrome
Other namesKRS
CausesMutations in the ATP13A2 gene
Frequency<1:1,000,000

Clinical

Symptoms include supranuclear gaze palsy, spasticity and dementia[1]. Other features include atypical parkinsonism with pyramidal signs and a characteristic minimyoclonus.

There is considerable variation in the phenotype.

Genetics

It is associated with mutations in the ATP13A2 gene. This gene is located on the short arm of chromosome 1 (1p36.13).

Mutations in this gene have also been associated with hereditary spastic paraplegia, uncomplicated early - or late-onset parkinsonism and neuronal ceroid lipofuscinosis.

History

It is named after Kufr Rakeb in Irbid, Jordan.

gollark: If we define Macron as the category Sh(S)Sh(S) of (set-valued) macrons on a (small) site SS, which is a Grothendieck topos, then the category of macrons on (C,J)(C,J) is the full subcategory of the category of premacrons.
gollark: As ever.
gollark: I was ABSOLUTELY RIGHT.
gollark: Remember when I said you should call the project Macron?
gollark: (I know you have one)

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.
Classification
External resources


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