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Dysmetria
- Autosomal dominant cerebellar ataxia, deafness, and narcolepsy (ADCADN) is a nervous system disorder with signs and symptoms that usually begin in mid-adulthood ...
- Autosomal recessive cerebellar ataxia type 1 (ARCA1) is a condition characterized by progressive problems with movement due to a loss (atrophy) of ... with movements that involve judging distance or scale (dysmetria). Other features of ARCA1 include abnormal eye movements ( ...
- Acute cerebellar ataxia is sudden inability to coordinate muscle movement due to disease or injury to the cerebellum. This is ... Acute cerebellar ataxia in children, particularly younger than age 3, may occur several days or weeks after an illness caused ...
- ... from the other copy of the gene. Aniridia, cerebellar ataxia, and mental retardation Aniridia-cerebellar ataxia-intellectual disability Aniridia-cerebellar ataxia-mental deficiency Partial ...
- ... affected individuals have problems with balance and coordination (cerebellar ataxia), often leading to difficulties with activities of daily ... of RNF216 protein function causes hypogonadotropic hypogonadism or cerebellar ataxia.The PNPLA6 gene provides instructions for making a ...
- ... signs and symptoms of the condition. Autosomal recessive cerebellar ataxia with mental retardation Autosomal recessive cerebellar hypoplasia with ... National Organization for Rare Disorders (NORD) ClinicalTrials.gov ... CEREBELLAR ATAXIA, IMPAIRED INTELLECTUAL DEVELOPMENT, AND DYSEQUILIBRIUM SYNDROME 1; CAMRQ1 ...
- ... of scar tissue in the liver (hepatic fibrosis); cerebellar ataxia, which is difficulty with coordination and balance arising ... Saldino disease MZSDS Renal dysplasia, retinal pigmentary dystrophy, cerebellar ataxia, and skeletal dysplasia Saldino-Mainzer dysplasia Saldino-Mainzer ...
- ... condition. CC2L Leukoencephalopathy with ataxia Leukoencephalopathy with mild cerebellar ataxia and white matter edema Leukoencephalopathy with white matter ...
- ... condition. Ataxia-hypogonadism-choroidal dystrophy syndrome BNHS BNS Cerebellar ataxia with hypogonadism and choroidal dystrophy syndrome Chorioretinal dystrophy, ...
- ... with a nervous system disorder called autosomal dominant cerebellar ataxia, deafness, and narcolepsy (ADCADN). Features of this disorder ... a methylation profile for DNMT1-associated autosomal dominant cerebellar ataxia, deafness, and narcolepsy. Clin Epigenetics. 2016 Sep 5; ...
