People with the more severe congenital form present from birth, might die at a very young age. In children it is called congenital myotonic dystrophy. Learn about the prognosis, life expectancy, and.
Myotonic dystrophy
An increased risk of death may be associated with younger age of onset, more severe muscle weakness, and cardiac conduction.
Ages and causes of death and the patients’ clinical features during lifetime were determined.
Though not curable, treatments options are available to help manage the. Myotonic dystrophy type 2 (dm2) is a dominantly inherited multisystem disease caused by a cctg repeat expansion in intron 1 of the cnbp gene. Muscular dystrophy life expectancy varies by different types and the severity of your symptoms. Life expectancy can vary for people with myotonic dystrophy.
Life expectancy in patients with dm2 is reduced, possibly attributable to multiple causes including increased risk of cardiac disease, pneumonia, and malignancies. Although in the last two. Life expectancy is greatly reduced in dm patients, particularly in those with early onset of the disease and proximal muscular involvement. Understand the different types of myotonic dystrophy, the impact on various body systems, and available medical interventions.
Many have a normal life expectancy.
We currently know of more than 10 different muscle disease types in the group of titinopathies, which can cause disorders both severe and mild, from prenatal death to very. Ta of all deceased patients with dm2 in the dutch neuromuscular database 2023. 8 life expectancy may be reduced for people with dm1. Titin abnormalities can cause a wide spectrum of muscle disorders called “titinopathy”.
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