Geniospasm
Encyclopedia
Geniospasm is movement disorder
of the mentalis
muscle.
It is a benign but socially excluding genetic disorder linked to chromosome 9q13-q21 where there are episodic involuntary up and down movements of the chin and lower lip. The movements consist of rapid fluttering or trembling at about 8Hz superimposed onto a once per three seconds movement of higher amplitude and occur symmetrically in the V shaped muscle. The tongue and buccal floor muscles may also be affected but to a much lesser degree.
The movements are always present but extreme episodes may be precipitated by stress, concentration or emotion and commence in early childhood. In some subjects social withdrawal and other compensatory behaviors occur.
The condition is extremely rare and in a study in 1999 only 23 families in the world were known to be affected, although due to embarrassment in afflicted individuals it may be under-reported. Inheritance is aggressively autosomal dominant. In at least two studies the condition appeared spontaneously in the families.
The condition responds very well to regular botulinus toxin injections into the mentalis muscle which paralyse the muscle but cause no impairment of facial expression or speech.
Movement disorder
Movement disorders include:* Akathisia * Akinesia * Associated Movements * Athetosis...
of the mentalis
Mentalis
The Mentalis is a paired central muscle of the lower lip, situated at the tip of the chin. It raises and pushes up the lower lip, causing wrinkling of the chin, as in doubt or displeasure...
muscle.
It is a benign but socially excluding genetic disorder linked to chromosome 9q13-q21 where there are episodic involuntary up and down movements of the chin and lower lip. The movements consist of rapid fluttering or trembling at about 8Hz superimposed onto a once per three seconds movement of higher amplitude and occur symmetrically in the V shaped muscle. The tongue and buccal floor muscles may also be affected but to a much lesser degree.
The movements are always present but extreme episodes may be precipitated by stress, concentration or emotion and commence in early childhood. In some subjects social withdrawal and other compensatory behaviors occur.
The condition is extremely rare and in a study in 1999 only 23 families in the world were known to be affected, although due to embarrassment in afflicted individuals it may be under-reported. Inheritance is aggressively autosomal dominant. In at least two studies the condition appeared spontaneously in the families.
The condition responds very well to regular botulinus toxin injections into the mentalis muscle which paralyse the muscle but cause no impairment of facial expression or speech.