myotonia congenita मीनिंग इन हिंदी

अधिक: आगे

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.

संज्ञा.

a mild, rare, congenital form of myotonia characterized by muscle stiffness
पर्याय: Thomsen''s disease