Summary
-
1.
The literature on hereditary cerebellar ataxia of childhood has been briefly reviewed.
-
2.
Two cases of hereditary cerebellar ataxia having pyramidal involvement, mental deficiency, pigmentation of the macular region in two brothers aged 9 and 7 years, respectively, are reported.
Similar content being viewed by others
References
Garland, H. andMoorhouse, D.—An extremely rare recessive hereditary syndrome including cerebellar ataxia, oligophrenia, cataracts and other features.J. Neurol, Neurosurg. and Psychiat.,16: 110, 1953.
Jervis, G. A.—Early familial cerebellar degeneration.J. Nerv. Ment. Dis.,3: 398, 1950.
Lamy, M. Grasset, A., Jammet, M. E. andViard, F. R.—Hereditary cerebellar ataxia of childhood.Arch. Franc. Pediat.,20: 5, 1963.
Norman, R. M.—Primary degeneration of the granular layer of the cerebellum. A unusual form of familial cerebellar atrophy occurring in early life.Brain,63: 365, 1940.
Scherer, H. J. cited byFord, F. R.—Diseases of the Nervous System in Infancy and Childhood and Adolescence.Charles Thomas Publisher, Springfield Illinois, 1960, 0. 378.
Sjogren.T.—Hereditary congenital spinocerebellar ataxia accompanied by congenital cataract and oligophrenia.Confina Neurol. 10: 293, 1950.
Stewart, R. M.—Amentia, familial cerebellar diplegia and retinitis pigmentosa.Proc. roy. Soc. Med.,30: 849, 1937.
Author information
Authors and Affiliations
Additional information
From the Department of Pediatrics, Gandhi Medical College, Bhopal.
Rights and permissions
About this article
Cite this article
Singh, S.D., Husain, S. Hereditary cerebellar ataxia, mental deficiency, pyramidal involvement and macular pigmentation. Indian J Pediatr 31, 355–358 (1964). https://doi.org/10.1007/BF02762219
Issue Date:
DOI: https://doi.org/10.1007/BF02762219