Essential tremor in families

genetics Essential tremor Family history

prof. dr. M.A.J. de Koning-Tijssen
Dr. A.M.M. van der Stouwe
drs. C.S.J. Everlo

Nature of the research:
The student will be joining our research project aimed at essential tremor, and will be involved in the inclusion of essential tremor families and their research measurements

Fields of study:
neurology genetics

Background / introduction
Tremor is one of the most common neurological disorders. It is an important topic in the Groningen Movement Disorders Group, as much remains to be unraveled concerning pathophysiology, diagnostic strategies and treatment.

Essential tremor is characterized by a bilateral, involuntary, rhythmic shaking (tremor) of the hands, occurring during movement or when the patient tries to maintain a specific position. The main phenotype includes tremor of the hands (in 97% of patients), voice (62%), head (48%), and to a lesser extent the jaw, tongue, legs and feet. The tremor can be very prominent, complicating simple activities of daily life such as drinking a cup of coffee and shaving, as well as compromising professional achievements in technical jobs such as electrician or watchmaker. Imagine a surgeon developing essential tremor: it would mean the end of his career. Another aspect is that some patients feel embarrassed in social situations such as dining in a restaurant, even to the extent that they would rather stay home.

Interestingly, half of the patients report a family history. As a consequence, it sometimes happens that one family member visits a neurologist and gets diagnosed, and in a little while the entire family is treated. In most affected families, essential tremor appears to inherit in an autosomal dominant pattern. However, in the search for a causal gene, only one very rare causal mutation and three susceptability loci have been found.

One of the proposed reasons for the poor outcome in genetic investigations so far is that the definition of essential tremor has not been applied critically. In other words, different types of tremor have been pooled in previous studies, and as a result no common mutations were found.

At the UMCG, we have conducted an imaging study with essential tremor patients, paying a lot of attention to diagnosing our patients correctly. Consequently, we have acquired a number of definite essential tremor patients, which could be used to study inheritability and genetics.
Research question / problem definition
1. Which disease features run in essential tremor families?
• Is alcohol responsivity a familial feature in essential tremor?
• Do neurophysiological features run in essential tremor families?
2. Can a familial phenotype be determined by clusterin of familial features?
3. If appropriately large affected families are found we will proceed to the third question: what are the genetics involved in these families?
The student will get in touch with patients that participated in, or applied for participation in our larger essential tremor study. The student will be involved in measurements of neurophysiological features and testing of alcoholresponsivity in essential tremor families.
Hopfner F, Haubenberger D, Galpern WR, Gwinn K, Van’t Veer A, White S, et al. Knowledge gaps and research recommendations for essential tremor. Park Relat Disord. 2016;33:27–35.

van der Stouwe AMM, Everlo CSJ, Tijssen MAJ. Which disease features run in essential tremor families? A systematic review. Park Relat Disord. 2019;69(September):71–8. Available from:
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