Congenital myasthenic syndrome

Congenital myasthenic syndrome (CMS) is an inherited neuromuscular disorder caused by defects of several types at the neuromuscular junction. The effects of the disease are similar to Lambert-Eaton Syndrome and myasthenia gravis, the difference being that CMS is not an autoimmune disorder. There are only 600 known family cases of this disorder and it is estimated that its overall frequency in the human population is 1 in 200,000.

Congenital myasthenic syndromes
SpecialtyNeurology 

Types

The types of CMS are classified into three categories: presynaptic, postsynaptic, and synaptic.

  • Presynaptic symptoms include brief stops in breathing, weakness of the eye, mouth, and throat muscles. These symptoms often result in double vision and difficulty chewing and swallowing.
  • Postsynaptic symptoms in infants include severe muscle weakness, feeding and respiratory problems, and delays in the ability to sit, crawl, and walk.
  • Synaptic symptoms include early childhood feeding and respiratory problems, reduced mobility, curvature of the spine, and weakness, which causes a delay in motor milestones.

Presentation

The onset of symptoms for all ages may include droopy eyelids. A particular form of postsynaptic CMS (slow-channel CMS) includes severe weakness beginning in infancy or childhood that progresses to respiratory problems, and leads to loss of mobility in adolescence or later life.

Mechanisms

Postsynaptic CMS

CMS is associated with genetic defects that affect proteins of the neuromuscular junction. Postsynaptic defects are the most frequent cause of CMS and often result in abnormalities in the acetylcholine receptor (AChR). In the neuromuscular junction there is a vital pathway that maintains synaptic structure and results in the aggregation and localization of AChR on the postsynaptic folds. This pathway consists of agrin, muscle-specific tyrosine kinase (MuSK), acetylcholine receptors (AChRs) and the AChR-clustering protein rapsyn, encoded by the RAPSN gene. The vast majority of mutations causing CMS are found in the AChR subunits and rapsyn genes.[1]

Out of all mutations associated with CMS, more than half are mutations in one of the four genes encoding the adult acetylcholine receptor (AChR) subunits. Mutations of the AChR often result in endplate deficiency. Most of the mutations of the AChR are mutations of the CHRNE gene. The CHRNE gene codes for the epsilon subunit of the AChR. Most mutations are autosomal recessive loss-of-function mutations and as a result there is endplate AChR deficiency. CHRNE is associated with changing the kinetic properties of the AChR.[2] One type of mutation of the epsilon subunit of the AChR introduces an Arginine into the binding site at the α/ε subunit interface of the receptor. The addition of a cationic Arg into the anionic environment of the AChR binding site greatly reduces the kinetic properties of the receptor. The result of the newly introduced Arg is a 30-fold reduction of agonist affinity, 75-fold reduction of gating efficiency, and an extremely weakened channel opening probability. This type of mutation results in an extremely fatal form of CMS.[3]

Another common underlying mechanism of CMS is the mutation of the rapsyn protein, coded by the RAPSN gene. Rapsyn interacts directly with the AChRs and plays a vital role in agrin-induced clustering of the AChR. Without rapsyn, functional synapses cannot be created, as the membrane folds do not form properly. Patients with CMS-related mutations of the rapsyn protein typically are either homozygous for N88K or heterozygous for N88K and a second mutation. The major effect of the mutation N88K in rapsyn is to reduce the stability of AChR clusters. The second mutation can be a determining factor in the severity of the disease.[1]

Studies have shown that most patients with CMS that have rapsyn mutations carry the common mutation N88K on at least one allele. However, research has revealed that there is a small population of patients who do not carry the N88K mutation on either of their alleles, but instead have different mutations of the RAPSN gene that codes for rapsyn on both of their alleles. Two novel missense mutations that have been found are R164C and L283P; the result is a decrease in co-clustering of AChR with raspyn. A third mutation is the intronic base alteration IVS1-15C>A, which causes abnormal splicing of RAPSN RNA. These results show that diagnostic screening for CMS mutations of the RAPSN gene cannot be based exclusively on the detection of N88K mutations[4]

Dok-7 is a postsynaptic protein that binds and activates MuSK protein, which then leads to AChR clustering and typical folding of the postsynaptic membrane. Mutations of Dok-7 are yrt another underlying mechanism of postsynaptic CMS.[5]

Diagnosis

Congenital myasthenic syndrome (CMS) is "often difficult to diagnose because of a broad differential diagnosis and lack of specific laboratory findings. Identification of the underlying mutation is critical, as certain mutations lead to treatment-responsive conditions while others do not."[6] Whole exome sequencing (WES) is often used as a diagnostic tool that allows for the "initiation of specific treatment".[6]

Management

Treatment depends on the form (category) of the disease. Although symptoms are similar to myasthenia gravis, treatments used in MG are not useful in CMS. MG is treated with immunosuppressants, but CMS is not an autoimmune disorder. Instead, CMS is genetic and responds to other forms of drug treatments. A form of presynaptic CMS is caused by an insufficient release of acetylcholine (ACh) and is treated with cholinesterase inhibitors.

Postsynaptic fast-channel CMS, in which ACh receptors do not stay open long enough, is treated with cholinesterase inhibitors and 3,4-diaminopyridine.[7][8] In the U.S., the more stable phosphate salt formulation of 3,4-diaminopyridine (amifampyridine phosphate) is under development as an orphan drug for CMS and is available to eligible patients at no cost under an expanded access program.[9][10] Postsynaptic slow-channel CMS is treated with quinidine or fluoxetine, which blocks the ACh receptor.

Ephedrine, a β(2)-adrenergic receptor agonist with alpha activity, has been tested on patients in clinical trials and appears to be an effective treatment for DOK7 CMS. Most patients tolerate this type of treatment and improvements in strength can be substantial. The effect of ephedrine is delayed and the improvement occurs over a period of months.[5][11]

Salbutamol, a selective β(2)-adrenergic receptor agonist, has been found, in adults, to have fewer side effects than Ephedrine and to be more easily obtained in some countries. It has been trialed in children with positive results[12]

As of 2022, the standard of care for DOK7 CMS is either ephedrine or salbutamol.[13]

People

Two brothers with apparent myasthenic syndrome with a seemingly circadian off/on cycle, living near Quetta, Pakistan were nicknamed the solar kids, because their condition resulted in an inability to move from approximately sunset to sunrise, while their daytime motor abilities were seemingly normal. Doctors observed that some "factor" seemed to become exhausted in the course of normal diurnal activities, and was "recharged" over the period of inertia and sleep. The father first sought help from spiritual healers, then turned to Western medicine. A younger brother of the two had also begun to manifest the same symptoms. The family had other children, two daughters and one son, who were unaffected. The "solar kids"' condition, despite extensive testing, was said to be undiagnosed as of 2016, and assumed to be genetic, as their parents were cousins. Samples of their genetic material were to be sent to the UK for analysis.[14][15][4][16]

See also

References
  1. Cossins, J.; Burke, G.; Maxwell, S.; Spearman, H.; Man, S.; Kuks, J.; Vincent, A.; Palace, J.; Fuhrer, C.; Beeson, D. (2006). "Diverse molecular mechanisms involved in AChR deficiency due to rapsyn mutations". Brain. 129 (10): 2773–2783. doi:10.1093/brain/awl219. PMID 16945936.
  2. Cheema, Usman (5 May 2016). "Rising and setting with the sun, Pakistan's 'solar kids' puzzle doctors". dawn.com. Retrieved 23 July 2016.
  3. Islamabad, Associated Press in (6 May 2016). "'Solar kids' who stop moving at night perplex doctors in Pakistan". theguardian.com. Retrieved 23 July 2016.
  4. "Peculiar ailment: The 'solar kids' of Mian Ghundi - Pakistan - Dunya News". dunyanews.tv. Retrieved 23 July 2016.
  5. Palace, J. (2012). "DOK7 congenital myasthenic syndrome". Annals of the New York Academy of Sciences. 1275 (1): 49–53. Bibcode:2012NYASA1275...49P. doi:10.1111/j.1749-6632.2012.06779.x. PMID 23278577. S2CID 8403500.
  6. Alvin Das; Dimitri Agamanolis; Bruce Cohen (8 April 2014). "Use of Next-Generation Sequencing as a Diagnostic Tool for Congenital Myasthenic Syndrome". Neurology. 51 (10): 717–20. doi:10.1016/j.pediatrneurol.2014.07.032. PMID 25194721. As with other rare childhood neurological conditions, CMS is often difficult to diagnose because of a broad differential diagnosis and lack of specific laboratory findings. Identification of the underlying mutation is critical, as certain mutations lead to treatment-responsive conditions while others do not. This case serves to highlight the importance of WES as a diagnostic tool that will assist in proper diagnosis, and in some circumstances, allow for initiation of specific treatment.
  7. Engel AG, et al. (April 2015). "Congenital myasthenic syndromes: pathogenesis, diagnosis, and treatment". Lancet Neurol. 14 (4): 420–34. doi:10.1016/S1474-4422(14)70201-7. PMC 4520251. PMID 25792100.
  8. Engel AG, et al. (2012). "New horizons for congenital myasthenic syndromes". Ann N Y Acad Sci. 1275 (1): 1275:54–62. Bibcode:2012NYASA1275...54E. doi:10.1111/j.1749-6632.2012.06803.x. PMC 3546605. PMID 23278578.
  9. "Search Orphan Drug Designations and Approvals". Archived from the original on 2015-05-21. Retrieved 2015-05-22.
  10. "Catalyst Using the Expanded Access Program to Conduct Phase IV Study with LEMS Patients". 2015-07-25. Archived from the original on 2015-07-25. Retrieved 2021-02-27.
  11. Lashley, D.; Palace, J.; Jayawant, S.; Robb, S.; Beeson, D. (2010). "Ephedrine treatment in congenital myasthenic syndrome due to mutations in DOK7". Neurology. 74 (19): 1517–1523. doi:10.1212/WNL.0b013e3181dd43bf. PMC 2875925. PMID 20458068.
  12. Burke, Georgina; Hiscock, Andrew; et al. (Feb 2013). "Salbutamol benefits children with congenital myasthenic syndrome due to DOK7 mutations". Neuromuscular Disorders. 23 (2): 170–175. doi:10.1016/j.nmd.2012.11.004. PMID 23219351. S2CID 15093159. Retrieved 1 February 2022.
  13. "Congenital myasthenic syndromes (treatment)". Genetic and Rare Diseases Information Center (GARD). National Institutes of Health (USA). Retrieved 1 February 2022.
  14. Junaidi, Ikram (2016-05-09). "'Solar kids' may have been diagnosed". DAWN. Archived from the original on 2016-05-17. Retrieved 2021-02-06.
  15. Associated Press (6 May 2016). "'Solar kids' who stop moving at night perplex doctors in Pakistan". The Guardian. Archived from the original on 2016-05-07. Retrieved 23 July 2016.
  16. "Pakistan's 'solar kids' baffle medical community". The Hindu. 5 May 2016. Retrieved 23 July 2016.{{cite news}}: CS1 maint: url-status (link)
  • Congenital Myasthenic Syndromes
  • About Congenital Myasthenic Syndrome From the Mayo Clinic
  • Treatment for Congenital Myasthenic Syndromes From the Mayo Clinic
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