Myotonia congenita is a congenital neuromuscular channelopathy that affects skeletal muscles (muscles used for movement). It is a genetic disorder. The...
26 KB (3,125 words) - 04:49, 26 July 2024
EMG. Myotonia is the defining symptom of many channelopathies (diseases of ion channel transport) such as myotonia congenita, paramyotonia congenita and...
16 KB (1,734 words) - 19:47, 25 July 2024
Paramyotonia congenita (PC) is a rare congenital autosomal dominant neuromuscular disorder characterized by "paradoxical" myotonia. This type of myotonia has been...
28 KB (2,477 words) - 21:27, 26 July 2024
fainting goat is an American breed of goat. It is characterised by myotonia congenita, a hereditary condition that may cause it to stiffen or fall over...
20 KB (2,576 words) - 20:50, 1 August 2024
to myotonia congenita, including muscle stiffness and cramping after initiating exercise (delayed muscle relaxation). However, it is pseudo-myotonia as...
14 KB (1,120 words) - 03:33, 20 May 2024
inherited human muscle disorders: recessive generalized myotonia congenita (Becker) and dominant myotonia (Thomsen). Chloride channel protein, skeletal muscle...
8 KB (998 words) - 23:47, 3 March 2023
Examples of atrophying muscle diseases include muscular dystrophy, myotonia congenita, and myotonic dystrophy. Changes in Na+ channel isoform expression...
8 KB (886 words) - 16:52, 24 March 2024
Mecasermin rinfabate (section Myotonia congenita)
products for treating this, or both. Myotonia congenita is a genetic muscle disorder. The two main types of myotonia congenita are Thomsen disease, which begins...
10 KB (1,227 words) - 01:32, 21 March 2024
e072885. doi:10.1136/bmj-2022-072885. ISSNĀ 1756-1833. S2CIDĀ 255570540. "Myotonia Congenita - Symptoms, Causes, Treatment | NORD". rarediseases.org. Retrieved...
69 KB (4,051 words) - 18:14, 10 July 2024