friedreich ataxias การใช้

• Symptoms are similar to those of Friedreich ataxia.
• Accordingly, MPP deficiency was shown to be involved in Friedreich ataxia, an autossomic recessive neurodegenerative disorder
• This form of ataxia is characterized by onset in the first 20 years, and is less severe than Friedreich ataxia.
• Degenerative diseases include parkinsonism, amyotrophic lateral sclerosis ( ALS ), multiple sclerosis, Huntington's disease, Niemann-Pick disease, and Friedreich ataxia.
• A Cochrane review on antioxidants and other pharmacological treatment of patients with Friedreich Ataxia, first published in 2012, is due to be updated before the end of 2015.
• Thirteen other syndromes may exhibit signs similar to Usher syndrome, including Alport syndrome, Alstrom syndrome, Bardet-Biedl syndrome, Cockayne syndrome, spondyloepiphyseal dysplasia congenita, Flynn-Aird syndrome, Friedreich ataxia, Hurler syndrome ( MPS-1 ), Kearns-Sayre syndrome ( CPEO ), Norrie syndrome, osteopetrosis ( Albers-Schonberg disease ), Refsum's disease ( phytanic acid storage disease ), and Zellweger syndrome ( cerebrohepatorenal syndrome ).