Karak syndrome

Karak syndrome is a neurological degenerative disorder involving excess cerebral iron accumulation.[1] The family who the disease was discovered in their siblings lived in Karak, a town in southern Jordan.[1] It is characterized by ataxia, inverted feet (talipes calcaneovarus), dysarthric scanning speech with dystonic features, dystonic movement of the tongue and facial muscles and choreiform movement was present in both upper and lower limbs, being more marked in the lower limbs, along with dystonic posture of the distal feet, bradykinesia present in both upper and lower limbs, dysmetria, dysdiadochokinesia, and intentional tremor were bilateral and symmetrical.[1]

Karak syndrome
SpecialtyNeurology

See also

References

  1. Mubaidin A, Roberts E, Hampshire D, et al. (July 2003). "Karak syndrome: a novel degenerative disorder of the basal ganglia and cerebellum". J. Med. Genet. 40 (7): 543–6. doi:10.1136/jmg.40.7.543. PMC 1735513. PMID 12843330. Retrieved 2009-07-07.
Classification
External resources
This article is issued from Wikipedia. The text is licensed under Creative Commons - Attribution - Sharealike. Additional terms may apply for the media files.