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abnormally long muscular contractions; slow relaxation of a muscle after a contraction

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出典(authority):フリー百科事典『ウィキペディア（Wikipedia）』「2018/03/20 16:42:01」(JST)

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Congenital myotonia, also called myotonia congenita, is a congenital neuromuscular channelopathy that affects skeletal muscles (muscles used for movement). It is a genetic disorder. The hallmark of the disease is the failure of initiated contraction to terminate, often referred to as delayed relaxation of the muscles (myotonia) and rigidity.^[1] Symptoms include delayed relaxation of the muscles after voluntary contraction (myotonia), and may also include stiffness, hypertrophy (enlargement), transient weakness in some forms of the disorder (from certain genetic mutations), and cramping. The condition is sometimes referred to as fainting goat syndrome, as it is responsible for the eponymous 'fainting' seen in fainting goats when presented with a sudden stimulus.

Symptoms

The prolonged muscle contractions, which occur most commonly in the leg muscles in recessive mutations, and more commonly in the hands, face, and eyelids in dominant mutations,^[2] are often enhanced by inactivity, and in some forms are relieved by repetitive movement known as "the warm-up effect". This effect often diminishes quickly with rest. Some individuals with myotonia congenita are prone to falling as a result of hasty movements or an inability to stabilize themselves after a loss of balance. During a fall, a person with myotonia congenita may experience partial or complete rigid paralysis that will quickly resolve once the event is over. However, a fall into cold water may render the person unable to move for the duration of submergence. As with myotonic goats, children are more prone to falling than adults, due to their impulsivity.

The two major types of myotonia congenita are distinguished by the severity of their symptoms and their patterns of inheritance. Becker disease usually appears later in childhood than Thomsen disease, and causes more severe myotonia, muscle stiffness and transient weakness.^[3] Although myotonia in itself is not normally associated with pain, cramps or myalgia may develop.^[3] People with Becker disease often experience temporary attacks of muscle weakness, particularly in the arms and hands, brought on by movement after periods of rest. They may also develop mild, permanent muscle weakness over time.^[4] This muscle weakness is not observed in people with Thomsen disease. However, in recent times, as more of the individual mutations that cause myotonia congenita are identified, these limited disease classifications are becoming less widely used.

Early symptoms in a child may include:

Difficulty swallowing
Gagging
Stiff movements that improve when they are repeated
Frequent falling
Difficulties opening eyelids after strenuous contraction or crying (von Graefe's sign)^[5]

Possible complications may include:

Aspiration pneumonia (caused by swallowing difficulties)
Frequent choking or gagging in infants (also caused by swallowing difficulties)
Abdominal muscle weakness
Chronic joint problems
Injury due to falls

Phenotypic variability

Both Thomsen and Becker myotonia have high phenotype variability. Severity of symptoms can vary greatly between individuals and throughout the lives of the individuals themselves. This may be partly because there are over 130 currently known different mutations that can cause the disorder, each with their own specifics, and also because myotonia congenita is an ion channel disorder, and ion channels are sensitive to internal and external environmental factors. It has been shown that pregnancy^[6] and the use of diuretics^[7] aggravate myotonia, and both these conditions are linked to the loss of divalent cations such as magnesium and calcium.^[8] It has further been shown that in pharmacological induced myotonia in isolated rat muscle, myotonia could be dampened by increasing the magnesium and calcium content of the extracellular medium.^[9] This has also been shown for isolated human muscle.^[10]

Adrenaline/epinephrine is well known to make myotonia worse in most individuals with the disorder, and a person with myotonia congenita may experience a sudden increase in difficulty with mobility in a particularly stressful situation during which adrenaline is released.

Due to the invisible nature of the disorder, the fact that those with myotonia congenita often appear very fit and able bodied, the general lack of knowledge about the disorder by the general and medical community, and often by the individual themselves, and the potential for inconsistency with the symptoms, many people with myotonia congenita have experienced a degree of social persecution at one time or another because of the effects of their disorder.

Temperature

Many patients report that temperature may affect the severity of symptoms, especially cold as being an aggravating factor.^[11] However, there is some scientific debate on this subject, and some even report that cold may alleviate symptoms.^[12]

The warm-up phenomenon

This phenomenon was described along with the disease by Thomsen in 1876 but its etiology remains unclear.

Patients report that myotonia congenita may present itself in the following ways (this is from first hand experience). If the person is sedentary and then decides to walk up a set of stairs, by the third or fourth step their leg muscles begin to stiffen significantly, requiring them to slow down almost to a complete stop. But as the muscles loosen up, a few steps later, they can once again begin to climb the steps at a normal pace. If this person plays any kind of a sport, a good warm-up is mandatory. Otherwise if they need to quickly and intensively use their muscles, such as in a sprint race or a basketball game, their muscles will freeze up, causing them to slow down or almost come to a complete stop. But once the muscles are warmed up, they can once again function normally. This can happen in various muscles, even in muscles such as the tongue. For example, if a person has not spoken for awhile and then wants to speak, their tongue may be stiff at first causing the words to come out a little garbled, but after a few seconds of trying to speak, the tongue muscle will loosen up and then they can speak normally for the remainder of the time that they are conversing.

Patients report that repeated contraction of muscle alleviates present myotonia with each contraction, such that myotonia is almost absent after a few contractions of the same muscle. The effect lasts about five minutes.^[13] There have been several proposed mechanisms for this phenomenon, but none have been conclusive; one theory is that the Na+/K+-ATPase is stimulated during the myotonic activity by increased intracellular Na⁺ in the cytosol of the muscle cell, increasing the activity of the Na+/K+-ATPase. However, in experiments with patients where the Na+/K+-ATPase had been blocked in the underarm by infusion of the Na+/K+-ATPase-blocker Ouabain, no effect on warm-up was observed.^[14] Another theory is that the few remaining functional chloride channels in muscle may become more active with increased muscle activity.^[15] However, this is not widely recognized.

It has been proposed that inactivation of Na⁺ channel 1.4 that resides in skeletal muscle, could play an important role in the warm-up phenomenon. In particular slow-inactivation of the channel is believed to have a spatial and temporal extend that is correlated to warm-up and therefore may provide a plausible cause.^[16]

Genetics

The disorder is caused by mutations in part of a gene (CLCN1) encoding the ClC-1 chloride channel, resulting in muscle fiber membranes having an unusually exaggerated response to stimulation (hyperexcitability).

Three cases have been reported who were diagnosed with Thomsen's myotonia and proved on genetic testing not to have mutations in the chloride gene but rather in the alpha-subunit of the voltage gated sodium channel (SCN4A).^[17] Like chloride channel mutations, patients with sodium channel mutations may have a very varied phenotype, making a diagnosis more difficult.

Pathophysiology

Myotonia congenita is caused in humans by loss-of-function mutations in the gene CLCN1. This is the gene encoding the protein CLCN1, that forms the ClC-1 chloride channel, critical for the normal function of skeletal muscle cells. This gene is also associated with the condition in horses and goats.

In short, in lack of sufficient functional chloride channels, the muscle fiber membrane becomes hyper-excitable and continues to be electrically active (firing action potentials) when stimulated, for longer periods of time, than a normal muscle fiber. This results in prolonged contraction/delayed relaxation of the muscle.

The dysfunctional Cl⁻ channels are located in the muscle fiber membrane and do not affect the motor nerve innervating the muscle. However, many studies have shown that denervation of muscle fibers alter the resting membrane conductance, but whether this affects myotonia in the muscle has been subject to heavy debate, and results from experiments are inconclusive.^[18]

In skeletal muscle fibers, a large transverse tubule system with a high surface-area to volume ratio exists. The onset of skeletal muscle activity is associated with the initiation and propagation of action potentials again associated with an efflux of K⁺ to the extracellular fluid and transverse tubule system. When many action potentials are elicited subsequently more K⁺ is expelled from the cell into the transverse tubular system. As K⁺ accumulates in the transverse tubular system the equilibrium potential for K⁺ (E_K⁺) normally around -80 mV, becomes more depolarized (depolarization), according to the Nernst equation. In skeletal muscle fibers the equilibrium potential for Cl⁻ is around -80 mV, equal to that of K⁺ at rest. Cl⁻ moves towards its equilibrium potential around -80 mV, while potassium moves towards its equilibrium potential more depolarized than -80 mV during activity. This results in a slightly more depolarized membrane potential of the fiber during repeated action potentials, see Goldman equation. The Na⁺ conductance is only elevated shortly compared to the K⁺ conductance during each action potential, which is why K⁺ largely determines the membrane potential (Cl⁻ is passively distributed during rest). In the case of myotonia congenita, the chloride channels that allow Cl⁻ to move across the membrane towards its equilibrium potential are defective, thus K⁺ is the only ion determining the membrane potential, and as more and more K⁺ accumulates in the transverse tubular system with each subsequent action potential the fiber depolarizes until the membrane potential comes close enough to the action potential threshold for spontaneous activity to ensue^[19] Spontaneous action potentials can arise for several seconds, leading to the delayed relaxation that is the hallmark of myotonia. Cessation of spontaneous activity is associated with sodium channel inactivation (Na_v1.4).

Diagnosis

Types

Two types of myotonia congenita exist, an autosomal dominant form and an autosomal recessive form. Autosomal dominant myotonia congenita (OMIM #160800) is also called Thomsen disease, after Danish/German physician Asmus Julius Thomas Thomsen (1815–1896), who himself had the disease and who wrote the first description of it in the medical literature (in 1876).^[20] Autosomal recessive myotonia congenita (OMIM #255700) is also called generalized myotonia, recessive generalized myotonia (RGM), Becker disease, and Becker myotonia, after the German professor Peter Emil Becker, who discovered its recessive nature.^[21]

The term congenital in its sense of "clinically apparent from birth" applies only to Thomsen disease, as the clinical onset of Becker myotonia may be delayed up to the age of 4 to 6 years.^[2] But in either form of myotonia congenita, the term's strictest sense reflects that the disease is genetically present from birth, although the clinical onset may be delayed.

With the advent of genetic testing, it has recently been found that some typically recessive mutations may occur in a dominant fashion in some individuals. The reason for this is not known.

Because several CLCN1 mutations can cause either Becker disease or Thomsen disease, doctors usually rely on characteristic signs and symptoms to distinguish the two forms of myotonia congenita. However, myotonia caused by CLCN1 mutations can occasionally be clinically indistinguishable from myotonia caused by sodium channel mutations (SCN4A mutations) resulting in the similar disease paramyotonia congenita.

A so-called Finnish heritage disease, congenital myotonia is more common in Finland and among ethnic Finns. A molecular study of the CLCN1 gene in 24 families in northern Finland, including 46 affected individuals, showed that although the inheritance appeared to be dominant (Thomsen type), in fact it is recessive (Becker type).^[22]

Other Disorders That May cause Myotonia or Similar Symptoms

Sodium channel myotonias (SCN4A)

Potassium-aggravated myotonia (acetazolamide responsive myotonia)
Paramyotonia congenita
Hyperkalemic periodic paralysis

Dystrophies

Myotonic dystrophy (myotonic muscular dystrophy: Type 1 and Type 2)

Potassium channel disorders (KCNJ2)

Andersen-Tawil syndrome

Other disorders

Thyroid disorders
Neuromyotonia (Isaacs Syndrome)
Schwartz–Jampel syndrome
Stiff person syndrome
Brody myopathy (Brody Disease, Brody's Disease, Brody's Myopathy)

Treatment

Some cases of myotonia congenita do not require treatment, or it is determined that the risks of the medication outweigh the benefits. If necessary, however, symptoms of the disorder may be relieved with quinine, phenytoin, carbamazepine, mexiletine and other anticonvulsant drugs. Physical therapy and other rehabilitative measures may also be used to help muscle function. Genetic counseling is available.

Prevalence

In northern Scandinavia, the prevalence of myotonia congenita has been estimated at 1:10,000.^[22]

Myotonia congenita is estimated to affect 1 in 1,000,000 people worldwide.^[23]

Research

Myotonia can be achieved in preparations of intact isolated muscle by the administration of 9-Anthracenecarboxylic acid a blocker of chloride channels.^[24]^[25] It is also possible to achieve myotonia in preparations of intact isolated muscle by greatly lowering or removing the extracellular content of chloride in the bathing medium.^[18]

During the 1970s several murine models of myotonia appeared. One in particular has been used widely, the adr mouse or "arrested development of righting response".^[26] This model is often used in scientific work with muscular dystrophy, and displays myotonia due to lack of functional chloride channels.

References

^ Gutmann, Laurie; Phillips Lh, Lawrence (2008). "Myotonia Congenita". Seminars in Neurology. 11 (3): 244–8. doi:10.1055/s-2008-1041228. PMID 1947487.
^ ^a ^b Lossin, Christoph; George, Alfred L. (2008). "Myotonia Congenita". In Rouleau, Guy; Gaspar, Claudia. Advances in Genetics. 63. pp. 25–55. doi:10.1016/S0065-2660(08)01002-X. ISBN 978-0-12-374527-9.
^ ^a ^b Rüdel, Reinhardt; Ricker, Kenneth; Lehmann-Horn, Frank (1988). "Transient weakness and altered membrane characteristic in recessive generalized myotonia (Becker)". Muscle & Nerve. 11 (3): 202–11. doi:10.1002/mus.880110303.
^ Becker, Peter Emil; Knussmann, Rainer; Kühn, Erich (1977). Myotonia congenita and syndromes associated with myotonia: clinical-genetic studies of the nondystrophic myotonias. Thieme. ISBN 978-3-13-224801-4. ^{[page needed]}
^ Wakeman, Bradley; Babu, Deepti; Tarleton, Jack; MacDonald, Ian M. (2008). "Extraocular muscle hypertrophy in myotonia congenita". Journal of American Association for Pediatric Ophthalmology and Strabismus. 12 (3): 294–6. doi:10.1016/j.jaapos.2007.12.002. PMID 18313341.
^ Basu, A.; Nishanth, P.; Ifaturoti, O. (2010). "Pregnancy in Women with Myotonia Congenita". Obstetric Anesthesia Digest. 30 (2): 135. doi:10.1097/01.aoa.0000370558.44941.91.
^ Bretag, A.H.; Dawe, S.R.; Kerr, D.I.B.; Moskwa, A.G. (1980). "Myotonia As a Side Effect of Diuretic Action". British Journal of Pharmacology. 71 (2): 467–71. doi:10.1111/j.1476-5381.1980.tb10959.x. PMC 2044474 . PMID 7470757.
^ Raman, Leela; Yasodhara, P.; Ramaraju, L.A. (1991). "Calcium and magnesium in pregnancy". Nutrition Research. 11 (11): 1231–6. doi:10.1016/S0271-5317(05)80542-1.
^ Skov, Martin; Riisager, Anders; Fraser, James A.; Nielsen, Ole B.; Pedersen, Thomas H. (2013). "Extracellular magnesium and calcium reduce myotonia in ClC-1 inhibited rat muscle". Neuromuscular Disorders. 23 (6): 489–502. doi:10.1016/j.nmd.2013.03.009. PMID 23623567.
^ Skov, M; De Paoli, FV; Lausten, J; Nielsen, OB; Pedersen, TH (January 2015). "Extracellular magnesium and calcium reduce myotonia in isolated ClC-1 chloride channel-inhibited human muscle". Muscle & nerve. 51 (1): 65–71. doi:10.1002/mus.24260. PMID 24710922.
^ Nielsen, VK; Friis, ML; Johnsen, T (1982). "Electromyographic distinction between paramyotonia congenita and myotonia congenita: Effect of cold". Neurology. 32 (8): 827–32. doi:10.1212/WNL.32.8.827. PMID 7201578.
^ Ricker, K.; Hertel, G.; Langscheid, K.; Stodieck, G. (1977). "Myotonia not aggravated by cooling". Journal of Neurology. 216 (1): 9–20. doi:10.1007/BF00312810. PMID 72799.
^ Birnberger, K. L.; Rüdel, R.; Struppler, A. (1975). "Clinical and electrophysiological observations in patients with myotonic muscle disease and the therapeutic effect of N-propyl-ajmalin". Journal of Neurology. 210 (2): 99–110. doi:10.1007/BF00316381. PMID 51920.
^ Van Beekvelt, Mireille C.P.; Drost, Gea; Rongen, Gerard; Stegeman, Dick F.; Van Engelen, Baziel G.M.; Zwarts, Machiel J. (2006). "Na+-K+-ATPase is not involved in the warming-up phenomenon in generalized myotonia". Muscle & Nerve. 33 (4): 514–23. doi:10.1002/mus.20483. PMID 16382442.
^ Pusch, Michael; Steinmeyer, Klaus; Koch, Manuela C.; Jentsch, Thomas J. (1995). "Mutations in dominant human myotonia congenita drastically alter the voltage dependence of the ClC-1 chloride channel". Neuron. 15 (6): 1455–63. doi:10.1016/0896-6273(95)90023-3. PMID 8845168.
^ Lossin, Christoph (2013). "Nav1.4 slow-inactivation: Is it a player in the warm-up phenomenon of myotonic disorders?". Muscle & Nerve. 47 (4): 483–7. doi:10.1002/mus.23713. PMID 23381896.
^ Trip J, Faber CG, Ginjaar HB, van Engelen BG, Drost G (2007) Warm-up phenomenon in myotonia associated with the V445M sodium channel mutation. J Neurol 254(2):257-258
^ ^a ^b Rüdel, R; Lehmann-Horn, F (1985). "Membrane changes in cells from myotonia patients". Physiological Reviews. 65 (2): 310–56. PMID 2580324.
^ Barchi, RL (1975). "Myotonia. An evaluation of the chloride hypothesis". Archives of Neurology. 32 (3): 175–80. doi:10.1001/archneur.1975.00490450055007. PMID 1119960.
^ Thomsen, J. (1876). "Tonische Krämpfe in willkürlich beweglichen Muskeln in Folge von ererbter psychischer Disposition". Archiv für Psychiatrie und Nervenkrankheiten. 6 (3): 702–18. doi:10.1007/BF02164912.
^ Becker, P. E. (1966). "Zur Genetik der Myotonien". In Kuhn, Erich. Progressive Muskeldystrophie Myotonie · Myasthenie. pp. 247–55. doi:10.1007/978-3-642-92920-5_32. ISBN 978-3-642-92921-2.
^ ^a ^b Papponen, H.; Toppinen, T.; Baumann, P.; Myllylä, V.; Leisti, J.; Kuivaniemi, H.; Tromp, G.; Myllylä, R. (1999). "Founder mutations and the high prevalence of myotonia congenita in northern Finland". Neurology. 53 (2): 297–302. doi:10.1212/WNL.53.2.297. PMID 10430417.
^ Emery, Alan E.H. (1991). "Population frequencies of inherited neuromuscular diseases—A world survey". Neuromuscular Disorders. 1 (1): 19–29. doi:10.1016/0960-8966(91)90039-U. PMID 1822774.
^ Moffett, RB; Tang, AH (1968). "Skeletal muscle stimulants. Substituted benzoic acids". Journal of Medicinal Chemistry. 11 (5): 1020–2. doi:10.1021/jm00311a023. PMID 5697062.
^ Villegas-Navarro, A; Martinez-Morales, M; Morales-Aguilera, A (1986). "Pharmacokinetics of anthracene-9-carboxylic acid, a potent myotonia-inducer". Archives Internationales de Pharmacodynamie et de Thérapie. 280 (1): 5–21. PMID 3718080.
^ Watts, R.L.; Watkins, J.; Watts, D.C. (1978). "A new mouse mutant with abnormal muscle function: Comparison with the Re‐dy mouse". The Biochemistry of Myasthenia Gravis and Muscular Dystrophy. London: Academic Press. pp. 331–4.

External links

GeneReview/NCBI/NIH/UW entry on myotonia congenita
NINDS: Myotonia congenita
National Library of Medicine: Myotonia congenita

UpToDate Contents

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1. デュシェンヌ型およびベッカー型筋ジストロフィーの臨床的特徴および診断 clinical features and diagnosis of duchenne and becker muscular dystrophy
2. 筋強直性ジストロフィー：病因、臨床的特徴、および診断 myotonic dystrophy etiology clinical features and diagnosis
3. デュシェンヌ型およびベッカー型筋ジストロフィーの治療 treatment of duchenne and becker muscular dystrophy
4. 筋強直性ジストロフィー：予後およびマネージメント myotonic dystrophy prognosis and management
5. 心疾患関連する遺伝性症候群 inherited syndromes associated with cardiac disease

English Journal

The differential diagnosis of myotonic syndromes: A case report-guided and neurophysiologic approach.

Cirillo G1, Todisco V1, Tedeschi G1.
Journal of the neurological sciences.J Neurol Sci.2016 Jan 15;360:98-9. doi: 10.1016/j.jns.2015.11.054. Epub 2015 Nov 30.
PMID 26723982

Studies on Chloride Channels and Their Modulators.

Patil VM, Gupta SP1.
Current topics in medicinal chemistry.Curr Top Med Chem.2015 Dec 14. [Epub ahead of print]
The prime role of mutations in the genes encoding chloride ion channels in various human diseases of muscle, kidney, bone and brain have been well established. It includes diseases such as myotonia congenita, dystrophia myotonica, cystic fibrosis, osteopetrosis, epilepsy as well as glioma progressio
PMID 26667116

Divalent cation-responsive myotonia and muscle paralysis in skeletal muscle sodium channelopathy.

Mankodi A1, Grunseich C2, Skov M3, Cook L4, Aue G4, Purev E4, Bakar D2, Lehky T5, Jurkat-Rott K6, Pedersen TH3, Childs RW4.
Neuromuscular disorders : NMD.Neuromuscul Disord.2015 Nov;25(11):908-12. doi: 10.1016/j.nmd.2015.08.007. Epub 2015 Aug 20.
We report a patient with paramyotonia congenita/hyperkalemic periodic paralysis due to Nav1.4 I693T mutation who had worsening of myotonia and muscle weakness in the setting of hypomagnesemia and hypocalcemia with marked recovery after magnesium administration. Computer simulations of the effects of
PMID 26494408

Japanese Journal

A Novel Mutation in the SCN4A Gene in a Japanese Family with Paramyotonia Congenita

Journal of Neurology & Neurophysiology 5(5), 1-3, 2014-09
NAID 120005567843

A large cohort of myotonia congenita probands : novel mutations and a high-frequency mutation region in exons 4 and 5 of the CLCN1 gene

Journal of human genetics 58(9), 581-587, 2013-09-01
NAID 10031195293

骨格筋型塩化物イオンチャネル遺伝子(CLCN1)の複合ヘテロ接合体変異で重症化したThomsen病

臨床神経学 53(4), 316-319, 2013-04
NAID 40019663429

Related Pictures

★リンクテーブル★

リンク元	「先天性筋緊張症」「先天性筋強直症」「generalized myotonia」
関連記事	「congenita」「myotonia」

「先天性筋緊張症」

Classification	V · T · D ICD-10: G71.1; ICD-9-CM: 359.2; OMIM: 160800; MeSH: D009224; DiseasesDB: 8736;
External resources	MedlinePlus: 001424;

Myotonia congenita
Specialty	neurology
	[edit on Wikidata]

　　[★]

英: congenital myotony
ラ: myotonia congenita、paramyotonia congenita
同: トムゼン病 Thomsen's disease, myotonia congenita Thomsen
関: 先天性パラミオトニー、先天性パラミオトニア、先天性筋強直症、全身性筋緊張、トムゼン病

「先天性筋強直症」

　　[★]

英: congenital myotonia
ラ: myotonia congenita
同: 先天性筋緊張症
関: 塩素イオンチャネル病

「generalized myotonia」

　　[★]

全身性筋強直、全身性筋緊張

関: myotonia congenita、Thomsen's disease

「congenita」

　　[★]

adj.

(後置するラテン語形容詞)先天性の

関: congenital、congenitally

ex.

dyskeratosis congenita、myotonia congenita

「myotonia」

　　[★] 筋緊張症、筋強直

[1] Gutmann, Laurie; Phillips Lh, Lawrence (2008). "Myotonia Congenita". Seminars in Neurology. 11 (3): 244–8. doi:10.1055/s-2008-1041228. PMID 1947487.

[Lossin_2008_25-55-2] Lossin, Christoph; George, Alfred L. (2008). "Myotonia Congenita". In Rouleau, Guy; Gaspar, Claudia. Advances in Genetics. 63. pp. 25–55. doi:10.1016/S0065-2660(08)01002-X. ISBN 978-0-12-374527-9.

[Rüdel_1988_202-11-3] Rüdel, Reinhardt; Ricker, Kenneth; Lehmann-Horn, Frank (1988). "Transient weakness and altered membrane characteristic in recessive generalized myotonia (Becker)". Muscle & Nerve. 11 (3): 202–11. doi:10.1002/mus.880110303.

[4] Becker, Peter Emil; Knussmann, Rainer; Kühn, Erich (1977). Myotonia congenita and syndromes associated with myotonia: clinical-genetic studies of the nondystrophic myotonias. Thieme. ISBN 978-3-13-224801-4. ^{[page needed]}

[5] Wakeman, Bradley; Babu, Deepti; Tarleton, Jack; MacDonald, Ian M. (2008). "Extraocular muscle hypertrophy in myotonia congenita". Journal of American Association for Pediatric Ophthalmology and Strabismus. 12 (3): 294–6. doi:10.1016/j.jaapos.2007.12.002. PMID 18313341.

[6] Basu, A.; Nishanth, P.; Ifaturoti, O. (2010). "Pregnancy in Women with Myotonia Congenita". Obstetric Anesthesia Digest. 30 (2): 135. doi:10.1097/01.aoa.0000370558.44941.91.

[7] Bretag, A.H.; Dawe, S.R.; Kerr, D.I.B.; Moskwa, A.G. (1980). "Myotonia As a Side Effect of Diuretic Action". British Journal of Pharmacology. 71 (2): 467–71. doi:10.1111/j.1476-5381.1980.tb10959.x. PMC 2044474 . PMID 7470757.

[8] Raman, Leela; Yasodhara, P.; Ramaraju, L.A. (1991). "Calcium and magnesium in pregnancy". Nutrition Research. 11 (11): 1231–6. doi:10.1016/S0271-5317(05)80542-1.

[9] Skov, Martin; Riisager, Anders; Fraser, James A.; Nielsen, Ole B.; Pedersen, Thomas H. (2013). "Extracellular magnesium and calcium reduce myotonia in ClC-1 inhibited rat muscle". Neuromuscular Disorders. 23 (6): 489–502. doi:10.1016/j.nmd.2013.03.009. PMID 23623567.

[10] Skov, M; De Paoli, FV; Lausten, J; Nielsen, OB; Pedersen, TH (January 2015). "Extracellular magnesium and calcium reduce myotonia in isolated ClC-1 chloride channel-inhibited human muscle". Muscle & nerve. 51 (1): 65–71. doi:10.1002/mus.24260. PMID 24710922.

[11] Nielsen, VK; Friis, ML; Johnsen, T (1982). "Electromyographic distinction between paramyotonia congenita and myotonia congenita: Effect of cold". Neurology. 32 (8): 827–32. doi:10.1212/WNL.32.8.827. PMID 7201578.

[12] Ricker, K.; Hertel, G.; Langscheid, K.; Stodieck, G. (1977). "Myotonia not aggravated by cooling". Journal of Neurology. 216 (1): 9–20. doi:10.1007/BF00312810. PMID 72799.

[13] Birnberger, K. L.; Rüdel, R.; Struppler, A. (1975). "Clinical and electrophysiological observations in patients with myotonic muscle disease and the therapeutic effect of N-propyl-ajmalin". Journal of Neurology. 210 (2): 99–110. doi:10.1007/BF00316381. PMID 51920.

[14] Van Beekvelt, Mireille C.P.; Drost, Gea; Rongen, Gerard; Stegeman, Dick F.; Van Engelen, Baziel G.M.; Zwarts, Machiel J. (2006). "Na+-K+-ATPase is not involved in the warming-up phenomenon in generalized myotonia". Muscle & Nerve. 33 (4): 514–23. doi:10.1002/mus.20483. PMID 16382442.

[15] Pusch, Michael; Steinmeyer, Klaus; Koch, Manuela C.; Jentsch, Thomas J. (1995). "Mutations in dominant human myotonia congenita drastically alter the voltage dependence of the ClC-1 chloride channel". Neuron. 15 (6): 1455–63. doi:10.1016/0896-6273(95)90023-3. PMID 8845168.

[16] Lossin, Christoph (2013). "Nav1.4 slow-inactivation: Is it a player in the warm-up phenomenon of myotonic disorders?". Muscle & Nerve. 47 (4): 483–7. doi:10.1002/mus.23713. PMID 23381896.

[Trip2007-17] Trip J, Faber CG, Ginjaar HB, van Engelen BG, Drost G (2007) Warm-up phenomenon in myotonia associated with the V445M sodium channel mutation. J Neurol 254(2):257-258

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myotonia congenita