|Title||Variants in SLC18A3, vesicular acetylcholine transporter, cause congenital myasthenic syndrome.|
|Publication Type||Journal Article|
|Year of Publication||2016|
|Authors||O'Grady, GL, Verschuuren, C, Yuen, M, Webster, R, Menezes, M, Fock, JM, Pride, N, Best, HA, Damm, TBenavides, Turner, C, Lek, M, Engel, AG, North, KN, Clarke, NF, MacArthur, DG, Kamsteeg, E-J, Cooper, ST|
|Date Published||2016 Oct 04|
|Keywords||Adolescent, Child, Diagnosis, Differential, Female, Genetic Variation, Humans, Male, Myasthenic Syndromes, Congenital, Vesicular Acetylcholine Transport Proteins|
OBJECTIVE: To describe the clinical and genetic characteristics of presynaptic congenital myasthenic syndrome secondary to biallelic variants in SLC18A3.
METHODS: Individuals from 2 families were identified with biallelic variants in SLC18A3, the gene encoding the vesicular acetylcholine transporter (VAChT), through whole-exome sequencing.
RESULTS: The patients demonstrated features seen in presynaptic congenital myasthenic syndrome, including ptosis, ophthalmoplegia, fatigable weakness, apneic crises, and deterioration of symptoms in cold water for patient 1. Both patients demonstrated moderate clinical improvement on pyridostigmine. Patient 1 had a broader phenotype, including learning difficulties and left ventricular dysfunction. Electrophysiologic studies were typical for a presynaptic defect. Both patients showed profound electrodecrement on low-frequency repetitive stimulation followed by a prolonged period of postactivation exhaustion. In patient 1, this was unmasked only after isometric contraction, a recognized feature of presynaptic disease, emphasizing the importance of activation procedures.
CONCLUSIONS: VAChT is responsible for uptake of acetylcholine into presynaptic vesicles. The clinical and electrographic characteristics of the patients described are consistent with previously reported mouse models of VAChT deficiency. These findings make it very likely that defects in VAChT due to variants in SLC18A3 are a cause of congenital myasthenic syndrome in humans.
|PubMed Central ID||PMC5075972|
|Grant List||UM1 HG008900 / HG / NHGRI NIH HHS / United States|