Myotonic dystrophy also known as dystrophia myotonica or myotonia atrophica, is an autosomal dominant hereditary multisystemic disease that is chronic, slow-progressing, and very variable. It's an illness that runs in families. A form of muscular dystrophyin which cataracts, heart conduction abnormalities, … See more There are two main types of myotonic dystrophy. Type 1 (DM1), also known as Steinert disease, is due to mutations (expansion) on the … See more Like most other dystrophies, there's no known cure for MD and thus, management is generally symptomatic. Physiotherapy has been indicated to improve ROM, prevent disuse atrophy, conserving energy, avoiding re-injury, and … See more DM affectation is essentially multisystemic, impacting most physiologic functions in the body of patients. Clinical presentation differs per DM type but type 2 is generally less severe than type 1. Some of the possible … See more WebFeb 6, 2024 · The term "muscular dystrophy" incorporates an assortment of hereditary disorders that lead to progressive, generalized disease of the muscle prompted by inadequate or missing glycoproteins in the muscle …

Myotonic Dystrophy: Types, Symptoms, Causes, and Treatment

WebFeb 11, 2024 · Overview. Muscular dystrophy is a group of diseases that cause progressive weakness and loss of muscle mass. In muscular dystrophy, abnormal genes (mutations) interfere with the production of proteins needed to form healthy muscle. There are many kinds of muscular dystrophy. Symptoms of the most common variety begin in childhood, … WebMyotonic dystrophy is an inherited neurological condition that causes progressive muscle weakness, muscle spasm, cataracts, cardiac abnormalities and endocrine disturbances. … blank line copy paste

About Myotonic Dystrophy - Genome.gov

WebThere are currently two clinically and molecularly defined forms of myotonic dystrophy: (1) myotonic dystrophy type 1 (DM1), also known as ‘Steinert’s disease'; and (2) myotonic dystrophy type 2 (DM2), also known as proximal myotonic myopathy. DM1 and DM2 are progressive multisystem genetic disorders with several clinical and genetic features in … WebMyotonic dystrophy is a genetic condition that causes progressive muscle weakness and wasting. It typically affects muscles of movement and commonly the electrical … WebDystrophic myotonia (DM) is a type of muscular dystrophy that causes muscle weakness and wasting over time. Types of DM include: Myotonic dystrophy type 1 (DM1). Myotonic … blank lined handwriting paper printable