Phenotypes for disease #00802 (CAMRQ1 (ataxia, cerebellar, mental retardation, quadrupedal locomotion, type 1 (CAMRQ-1)), OMIM:224050)

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0000043861 At 22 months of age, the patient showed global hypotonia, truncal ataxia, nystagmus, intentional tremor, dysmetria and motor delay. At age of 12 years mild dysarthria, moderate intellectual impairment and mild ataxia gait were present, nystagmus was absent and walking without support. MRI, performed at 3 and 9 years of age, showed marked but not progressive ponto-cerebellar hypoplasia associated to mild simplification of cortical gyration - - Familial, autosomal recessive - - - - - Enza Maria Valente 00057180
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