
Myotonic dystrophy - Wikipedia
Myotonic dystrophy (DM) is a genetic condition that is inherited in an autosomal dominant pattern, meaning each child of an affected individual has a 50% chance of inheriting the disease. The mutation involves satellite DNA , which is tandemly repeated sequences of …
Myotonic Dystrophy (DM) - Diseases - Muscular Dystrophy …
Myotonic dystrophy (DM) is a form of muscular dystrophy that affects muscles and many other organs in the body. The word “myotonic” is the adjectival form of the word “myotonia,” defined as an inability to relax muscles at will.
Myotonic Dystrophy: What It Is, Symptoms, Types & Treatment
Dec 12, 2022 · Myotonic dystrophy (DM) is an inherited multisystem condition that mainly causes progressive muscle loss, weakness and myotonia. It can also affect other parts of your body, including your heart, lungs and eyes. There’s no cure for DM, but certain treatments and therapies can help manage symptoms and improve quality of life.
Myotonic Dystrophy - StatPearls - NCBI Bookshelf
Jun 26, 2023 · Myotonic dystrophy is a rare progressive disorder that universally presents with weakness. In addition to musculoskeletal weakness, cardiac conduction defects and early cataracts are common. There are two distinct forms of myotonic dystrophy: DM1 and DM2.
Myotonic dystrophy | About the Disease | GARD - Genetic and …
Myotonic dystrophy is a disease that affects the muscles and other body systems. It is the most common form of muscular dystrophy that begins in adulthood, usually in a person's 20s or 30s. This disease is characterized by progressive muscle loss and weakness.
Myotonic Dystrophy: Types, Symptoms, Causes, and Treatment - WebMD
Jun 5, 2024 · Myotonic dystrophy causes muscle wasting and weakness that gets worse over time. These symptoms can make it hard to relax your muscles after gripping or holding something. At least 1...
Myotonic Dystrophy Type 1 - GeneReviews® - NCBI Bookshelf
Sep 17, 1999 · Myotonic dystrophy type 1 (DM1) is a multisystem disorder that affects skeletal and smooth muscle as well as the eye, heart, endocrine system, and central nervous system. The clinical findings, which span a continuum from mild to severe, have been categorized into three somewhat overlapping phenotypes: mild, classic, and congenital.
Myotonic Dystrophy: Disease Repeat Range, Penetrance, Age of …
Myotonic dystrophy (DM) is an autosomal dominant neuromuscular disease primarily characterized by myotonia and progressive muscle weakness. The pathogenesis of DM involves microsatellite expansions in noncoding regions of transcripts that result in …
What is Myotonic Dystrophy?
Mar 21, 2025 · Myotonic dystrophy (DM) is a multi-systemic inherited disease that affects at least 1 in 2,100 people or over 150,000 individuals in the US alone (Johnson 2021).
Myotonic dystrophy: Types, causes, symptoms, treatments
Mar 19, 2024 · Myotonic dystrophy is a condition that causes thinned muscles, decreased muscle tone, and muscle weakness. Over time, a person may lose their strength and have issues...