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Spasmodic dysphonia, also known as laryngeal dystonia, is a disorder in which the muscles that generate a person's voice go into periods of spasm. [1] [2] This results in breaks or interruptions in the voice, often every few sentences, which can make a person difficult to understand. [1]
Causes distortions of the mouth and tongue. Spasmodic dysphonia/Laryngeal dystonia muscles of larynx: Causes the voice to sound broken, become hoarse, sometimes reducing it to a whisper. Focal hand dystonia (also known as musician's or writer's cramp). single muscle or small group of muscles in the hand
Multiple factors cause the muscles of the larynx to become tense. This changes the position of the larynx and affects the cartilaginous structures within the larynx leading to abnormal phonation. [3] There is increased muscle activity in MTD due to personal temperament, increased vocal use, and underlying medical or physical causes. [3]
The spasms may cause the mouth to pull open, shut tight, or move repetitively. Speech and swallowing may be distorted. It is often associated with dystonia of the cervical muscles (Spasmodic Torticollis), eyelids (Blepharospasm), or larynx (Spasmodic Dysphonia). [citation needed]
Laryngospasm is an uncontrolled or involuntary muscular contraction of the vocal folds. [1] It may be triggered when the vocal cords or the area of the trachea below the vocal folds detects the entry of water, mucus, blood, or other substance.
The diagnosis of focal dystonia is highly dependent on the history of the patient, as physical exam is typically normal, and ruling out other causes of movement disorder. [10] [11] The main types of are blepharospasm, oromandibular dystonia, spasmodic dysphonia, spasmodic torticollis, and limb dystonia, all affecting a different region of the ...
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This autosomal-dominant condition is the most frequent cause of dopamine-responsive dystonia. [1] Mutations in the gene for tyrosine hydroxylase may lead to tyrosine hydroxylase deficiency, a rare form of dopamine-responsive dystonia inherited in an autosomal recessive manner. [ 2 ]