myotonia congenita sentence in Hindi
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- The characteristic is caused by a hereditary genetic disorder called myotonia congenita.
- Two patients initially diagnosed with fibromyalgia were subsequently shown to have myotonia congenita.
- Fainting goats have a muscle condition called myotonia congenita.
- They also have a muscle condition called myotonia congenita.
- Examples of atrophying muscle diseases include muscular dystrophy, myotonia congenita, and myotonic dystrophy.
- The two major types of myotonia congenita are distinguished by the severity of their symptoms and their patterns of inheritance.
- In myotonia congenita, the term reflects that the disease is genetically present from birth, while the onset may be delayed.
- Both patients had been seen by skeletal muscle chloride channel which is the underlying cause of myotonia congenita revealed that both patients had mutations in this gene.
- The channelopathies of human skeletal muscle include hyper-and hypokalemic ( high and low potassium blood concentrations ) periodic paralysis, myotonia congenita and paramyotonia congenita.
- 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.
- According to Phillip Sponenberg, an authority on myotonia congenita and Tennessee fainting goats, myotonia has been extensively studied in humans and somewhat less extensively in other species.
- 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.
- Mexiletine may also be of use in patients experiencing refractory pain and is also effective for treating muscle stiffness resulting from myotonic dystrophy ( Steinert's disease ) or nondystrophic myotonias such as myotonia congenita ( Thomsen disease ).
- Hypermobility may be symptomatic of a serious medical condition, such as Stickler Syndrome, Ehlers-Danlos syndrome, Marfan syndrome, Loeys-Dietz syndrome, rheumatoid arthritis, osteogenesis imperfecta, polio, Down syndrome, morquio syndrome, cleidocranial dysostosis or myotonia congenita.
- :I don't know anything about this particular child, but the symptom and the fact that he's German suggest Myotonia congenita, a channelopathy resulting in tonic contraction of skeletal muscles ( which constantly " exercises " them ) . rekcut 14 : 41, 24 May 2007 ( UTC)
- 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.
- 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.
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