LINGO1 VARIANT INCREASES RISK OF FAMILIAL ESSENTIAL TREMOR
نویسندگان
چکیده
منابع مشابه
Familial aggregation of cranial tremor in familial essential tremor.
BACKGROUND Essential tremor (ET) is often familial and phenotypic features may be shared within families. Cranial (neck, voice, and jaw) tremor is an important feature of ET. We examined whether cranial tremor aggregates in ET families, after controlling for other factors (age, tremor severity, and duration). METHODS Among ET probands and relatives enrolled in a genetic study at Columbia Univ...
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The most frequent MAPT H1 haplotype is associated with the risk for developing progressive supranuclear palsy and other neurodegenerative diseases such as Parkinson's disease. A recent report suggests that the MAPT H1 is associated with the risk for developing essential tremor. We wanted to confirm this association in a different population. We analyzed the distribution of allelic and genotype ...
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Essential tremor (ET) and Parkinson's disease (PD) are two of the most common adult onset movement disorders with overlapping clinical features. PD patients with leucine-rich repeat kinase-2 (LRRK2) mutations may present initially with an ET phenotype. To address the possibility of a common genetic link between ET and PD, we examined the association between a common LRRK2 R1628P gene variant an...
متن کاملFamilial Aggregation of the Cerebellar Signs in Familial Essential Tremor
BACKGROUND Although the hallmark feature of essential tremor (ET) is kinetic tremor, patients may exhibit additional motor features (e.g., intention tremor and mild gait ataxia) that are markers of an underlying abnormality of cerebellar function. ET is also a highly familial disorder, but we do not know whether the presence and expression of cerebellar signs are similar across family members. ...
متن کاملEssential (familial, hereditary) tremor: a case report.
OF PATHOLOGICAL FINDINGS Striatun, Subst. nigra Red nucleus Cerebellum Case 1 Numerical Hassler (1939) reduction of small cells in caudate and putamen Case 2 Reduction of Hassler (1939) small cells. Small softenings in caudate and putamen Case 3 Fibrillar gliosis Mylle and van in pallidum Bogaert (1940) Case 4 Atrophy of Mylle and van putamen and Bogaert ( 1948) caudate-6tat cribl6, small softe...
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ژورنال
عنوان ژورنال: Neurology
سال: 2009
ISSN: 0028-3878,1526-632X
DOI: 10.1212/wnl.0b013e3181bacfc9