Unknown

Dataset Information

0

A presynaptic congenital myasthenic syndrome attributed to a homozygous sequence variant in LAMA5.


ABSTRACT: We report a severe defect of neuromuscular transmission in a consanguineous patient with a homozygous variant in the laminin ?5 subunit gene (LAMA5). The variant c.8046C > T (p.Arg2659Trp) is rare and has a predicted deleterious effect. The affected individual, who also carries a rare homozygous sequence variant in LAMA1, had normal cognitive function, but magnetic resonance brain imaging showed mild volume loss and periventricular T2 prolongation. Repetitive nerve stimulation at 2 Hz showed 50% decrement of compound muscle action potential amplitudes but 250% facilitation immediately after exercise, similar to that seen in Lambert-Eaton myasthenic syndrome. Endplate studies demonstrated a profound reduction of the endplate potential quantal content but normal amplitudes of miniature endplate potentials. Electron microscopy showed endplates with increased postsynaptic folding that were denuded or only partially occupied by small nerve terminals. Expression studies revealed that p.Arg2659Trp caused decreased binding of laminin ?5 to SV2A and impaired laminin-521 cell adhesion and cell projection support in primary neuronal cultures. In summary, this report describing severe neuromuscular transmission failure in a patient with a LAMA5 mutation expands the list of phenotypes associated with defects in genes encoding ?-laminins.

SUBMITTER: Maselli RA 

PROVIDER: S-EPMC6252105 | biostudies-literature | 2018 Feb

REPOSITORIES: biostudies-literature

altmetric image

Publications

A presynaptic congenital myasthenic syndrome attributed to a homozygous sequence variant in LAMA5.

Maselli Ricardo A RA   Arredondo Juan J   Vázquez Jessica J   Chong Jessica X JX   Bamshad Michael J MJ   Nickerson Deborah A DA   Lara Marian M   Ng Fiona F   Lo Victoria Lee VL   Pytel Peter P   McDonald Craig M CM  

Annals of the New York Academy of Sciences 20180128 1


We report a severe defect of neuromuscular transmission in a consanguineous patient with a homozygous variant in the laminin α5 subunit gene (LAMA5). The variant c.8046C > T (p.Arg2659Trp) is rare and has a predicted deleterious effect. The affected individual, who also carries a rare homozygous sequence variant in LAMA1, had normal cognitive function, but magnetic resonance brain imaging showed mild volume loss and periventricular T2 prolongation. Repetitive nerve stimulation at 2 Hz showed 50%  ...[more]

Similar Datasets

| S-EPMC5541137 | biostudies-literature
| S-EPMC5413866 | biostudies-other
| S-EPMC6014458 | biostudies-literature
| S-EPMC5011057 | biostudies-literature
| S-EPMC7959540 | biostudies-literature
| S-EPMC5617158 | biostudies-literature
| S-EPMC7029005 | biostudies-literature
| S-EPMC10668953 | biostudies-literature
| S-EPMC10074331 | biostudies-literature