Abstract
Recent advances in molecular biology have ushered in a new era of Neurology. In recent years, more and more genetic diseases have been diagnosed based on molecular tests. As infectious diseases of the nervous system such as poliomyelitis decrease in a given population, a larger proportion of neurological disorder encountered have a genetic basis. In a review of referral patterns to tertiary genetic centers in India, Verma et al (2003) found that a high percentage of referrals to molecular diagnostic laboratories are for neurological conditions. Duchenne muscular dystrophy (12.5%), Fragile X syndrome (10.3%), spinal muscular atrophy (8.9%), triplet repeat disorders-spinocerebellar ataxias, Huntington disease and Friedreich ataxia (4.6%) and mitochondrial disorders (2.9%) account for about 40% of all referrals.
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Further Reading
Baraitser M (1997The Genetics of Neurological Disorders, Oxford University Press, Oxford
Pulst Stefan-M (2000) Ed.Neurogenetics, Contemporary Neurology Series, Oxford University Press, New York and Oxford.
Harper PS (2001Myotonic Dystrophy,ed 3. WB Saunders, London.
Harper PS (2002Huntington’s Disease, ed3. Oxford University Press, Oxford.
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Emery AEH (2001) ed. The Muscular Dystrophies, Oxford University Press
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Kumar, D., Patton, M.A., Kumar, A. (2004). Genetic Neurological and Psychiatric Diseases. In: Kumar, D. (eds) Genetic Disorders of the Indian Subcontinent. Springer, Dordrecht. https://doi.org/10.1007/978-1-4020-2231-9_16
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