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• Conditions (26): Angelman syndrome, Marfan syndrome, Darier's Disease, and 23 others Angelman syndrome, Marfan syndrome, Darier's Disease, Rett syndrome, Retinitis Pigmentosa, von Willebrand Disease, Tuberous Sclerosis, Huntington's disease, Wiskott-Aldrich Syndrome, Ataxia Telangiectasia, Polycystic Kidney Diseases, Hereditary Diseases, Alport's syndrome, Adrenoleukodystrophy, Apert-Crouzon syndrome, Congenital ichthyosis, Werner Syndrome, Von Hippel-Lindau Syndrome, Muscular Dystrophies, Multiple Endocrine Neoplasia, Nephroblastoma, Congenital chromosomal disease, Neurofibromatoses, Testicular Feminization, Usher Syndromes, Li-Fraumeni Syndrome [hide]
• Groups (59): Friedreich's Ataxia, Hemophilia, HD, and 56 others Friedreich's Ataxia, Hemophilia, HD, Agenesis of Corpus Callosum, Dandy Walker Syndrome, Pachygyria, Empty Sella Syndrome, Anencephaly, hydrocephalus, Trigeminal Neuralgia, Arnold Chiari Malformation, Spinal Stenosis, Hashimoto's Encephalopathy, Tourette Syndrome, Wernicke-Korsakoff Syndrome, Parkinson's Disease, Darier's Disease, Achalasia, Osteogenesis Imperfecta, Rare 'Orphan' Disorders, Polycystic Kidney Diseases, Hirschsprung's Disease, PANDAS Syndrome, Dercum's Disease, Trimethylaminuria, Addison's Disease, Blepharophimosis, Fragile X Syndrome, Ledderhose Disease, Aarskog Syndrome, Legg-Calve-Perthes Disease, Microphthalmia, Cri-du-Chat Syndrome, Behcet's Syndrome, Cleidocranial Dysplasia, Fructose Intolerance, 1p36 Deletion Syndrome, Kartagener Syndrome, Cushing's Syndrome, Menkes Kinky Hair Syndrome, Androgen Insensitivity Syndrome, Esophageal Atresia and/or Tracheosophageal Fistula, Short Bowel Syndrome, Adrenoleukodystrophy, Simpson-Golabi-Behmel Syndrome, Diabetes Insipidus, Multiple Endocrine Neoplasia Type 1, Polycythemia Vera, Factor V Leiden, Lupus, Lichen Sclerosis, Beckers Nevus, Sweet Syndrome, Retroperitoneal Fibrosis, Large Granular Lymphocyte Leukemia, Dyslexia, Post-Polio Syndrome, Astrocytoma, Adie Syndrome [hide]
• Symptoms (25): Von Willebrand disease, Organic brain syndrome, Kallmann Syndrome, and 22 others Von Willebrand disease, Organic brain syndrome, Kallmann Syndrome, Gilles de la Tourette syndrome, Wernicke-Korsakoff Syndrome, Ataxia, Mental Retardation, Blepharophimosis, Cerebellar Ataxia, Myoclonus, Sweet Syndrome, Club Foot, Scleroderma, pyoderma gangrenosum, cerebellar ataxia/dyskinesia, Castleman's Disease, Multiple Organ Failure, Intracranial Pressure, Polymicrogyria, Tetralogy of Fallot, Tethered Spinal Cord, Glioma, neuropathy, Symptoms and Side Effects, Mitochondrial Myopathy [hide]
• Treatments (1): achondroplasia achondroplasia [hide]

About Friedreich's Ataxia

Friedreich's ataxia is an inherited disease that causes progressive damage to the nervous system resulting in symptoms ranging from gait disturbance and speech problems to heart disease. "Ataxia," which refers to coordination problems such as clumsy or awkward movements and unsteadiness, occurs in many... more

Friedreich's ataxia is an inherited disease that causes progressive damage to the nervous system resulting in symptoms ranging from gait disturbance and speech problems to heart disease.
"Ataxia," which refers to coordination problems such as clumsy or awkward movements and unsteadiness, occurs in many different diseases and conditions. The ataxia of Friedreich's ataxia results from the degeneration of nerve tissue in the spinal cord and of nerves that control muscle movement in the arms and legs. The spinal cord becomes thinner and nerve cells lose some of their myelin sheath (the insular covering on all nerve cells that helps conduct nerve impulses).
Delatycki et al. (2000) provided an overview of the clinical features, pathology, molecular genetics, and possible therapeutic options in Friedreich ataxia.

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