What is Friedreich ataxia?
Friedreich ataxia is a genetic condition that affects the nervous system and causes movement problems. People with this condition develop impaired muscle coordination (ataxia) that worsens over time.
What is Friedreich ataxia?
Friedreich ataxia is a disease of the central nervous system.
The nervous system in the body can be divided into 2 categories: the central nervous system and the peripheral nervous system.
The neural degenerative condition of Friedreich ataxia was present in the patient reported by Miyamoto et al. (1999). There are other conditions involving neuropathy of peripheral nerves that have been associated with hearing loss and ANSD.
C-reactive protein, Vasomotor, Dental Economics, Distraction Osteogeneses, Dithizon, Entomopoxviruses, Epoxylite-9075, Erythrocyte Membrane Anion Transport Protein, Facial Spasms, Unilateral, Fitzgerald Factor, Friedreich Ataxia, ...
Prior to the description of ABL in 1950, it is believed that people with ABL were diagnosed as having either Friedreich ataxia (a more common form of hereditary ataxia) or some other neurologic disorder.
neuropathiesincluding Charcot-Marie-Tooth disease, Guillain-Barré syndrome, chronic inflammatory demyelinating polyradiculoneuropathy (CIDP) and Friedreich ataxia
traumatic nerve injuriesincluding accidents and sports injuries ...
ataxia with isolated vitamin E deficiency
AVED
familial isolated vitamin E deficiency
FIVE
Friedreich ataxia phenotype with selective vitamin E deficiency
Friedreich-like ataxia
Vitamin E Deficiency ...
Turner's syndrome, a genetic disease in females that affects physical and reproductive development.
Other diseases that can cause scoliosis are Marfan's syndrome, Aicardi syndrome, Friedreich ataxia, Albers-Schonberg disease, rheumatoid arthritis, ...
Friedreich ataxia -- congenital glaucoma ... slurred speech, slow speech, speech problems
Friedreich's ataxia ... slurred speech, speech problems
Frontotemporal dementia ... altered speech output, mutism, stuttering
Frostbite ... slurred speech ...
 See also: Ataxia, Autosomal recessive, Symptom, Deficiency, Central nervous system
  
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