Cerebellar Degeneration with Slow Movements& 333i81d nbsp; & 333i81d nbsp; & 333i81d nbsp; & 333i81d nbsp; & 333i81d nbsp; & 333i81d nbsp; & 333i81d nbsp; & 333i81d nbsp; & 333i81d nbsp; & 333i81d nbsp; & 333i81d nbsp; & 333i81d nbsp; & 333i81d nbsp; & 333i81d nbsp; & 333i81d nbsp; & 333i81d nbsp; & 333i81d nbsp; & 333i81d nbsp; & 333i81d nbsp; & 333i81d nbsp; 221
General: Autosomal dominant; described only in Indian families; associated with spinocerebellar degeneration and abnormal eye movements.
Ocular: Paramedian pontine reticular formation (horizontal gaze center); absent rapid movements of both eyes and abnormally slow movements.
Clinical: Brainstem lesion of paramedian pontine reticular formation; progressive mental deterioration.
McKusick VA. Mendelian Inheritance in Man; A Catalog of Human Genes and Genetic Disorders, 12th ed. Baltimore: The Johns Hopkins University Press, 1998.
Online Mendelian Inheritance in Man, OMIM. McKusick-Nathans Institute for Genetic Medicine, Johns Hopkins University and National Center for Biotechnology Information, National Library of Medicine, February 12, 2007. World Wide Web URL: https://www.ncbi.nlm.nih.gov/omim/.
Wadia NH, et al. A new form of heredofamilial spinocerebellar degeneration with slow eye movements. Brain 1971; 94:359-374.
Linear Nevus Sebaceus of Jadassohn (Nevus Sebaceus of Jadassohn; Jadassohn-Type Anetoderma; Organoid Nevus syndrome; Sebaceus nevus syndrome ) [...] |
Neurocutaneous Syndrome [...] |
Ocular Dominance [...] |
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