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Friedreich's ataxia
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    Also found in: Medical, Encyclopedia, Wikipedia 0.02 sec.

Friedreich's ataxia

Rare inherited neurological disorder characterized by unsteadiness of gait and posture and spasticity of the limbs. It is a progressive condition, with onset usually around the age of 12. Victims rarely live beyond the age of 40.

It is the result of a ‘stutter’ within a gene where one codon repeats itself. The disease affects 1 in 50,000 Europeans.



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? Mentioned in ? References in periodicals archive
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age/sex disease Aevaliotis et al, 1985 (7) 3 wk/F None Wang, 1987 (6) 17 mo/M Congenital heart disease Tristram and Forbes, 1988 (8) 11 mo/F Vesicoureteral reflux Dollberg et al, 1990 (4) 5 yr/F None Yogev and Kozlowski 13 yr/M Friedrich's ataxia 1990 (5) Ortega Calvo et al, 1999 (9) 10 y/F Proteinuria Brooks and Feldman, 2003, 17 yr/F Ewing's sarcoma present ease Clinical Source of Case report (ref.
Central venous catheter infection in a child: case report and review ... by Feldman, Sandor / Southern Medical Journal
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