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1. • • Myotonic dystrophy type 2 (DM2) is characterized by myotonia and muscle dysfunction (proximal and axial weakness, myalgia, and stiffness), and less commonly by posterior subcapsular cataracts, cardiac conduction defects, insulin-insensitive type 2 diabetes mellitus, and other endocrine abnormalities.
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     Myotonic Dystrophy Type 2 - GeneReviews® - NCBI Bookshelf

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   What are the symptoms of mild myotonic dystrophy?

   • In mild myotonic dystrophy type one, symptoms are usually less intense. With the congenital form, people may have weak muscle tone, breathing problems, clubfoot (an inward and upward turning of their foot ), intellectual disability, or delayed development. Some of these symptoms could be fatal. Myotonic dystrophy type two.

   Myotonic Dystrophy: Types, Symptoms, Causes, and Treatment - WebMD

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   What are the symptoms of myotonic dystrophy in DM1 and DM2?

   • The symptoms of myotonic dystrophy in DM1 and DM2 generally include: DM1 can also include signs of intellectual disability, though this is not typically the case with DM2. Myotonic dystrophy can also lead to conditions such as type 2 diabetes and cataracts.

   Myotonic dystrophy: Types, causes, symptoms, treatments

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   What is myotonic dystrophy type 2?

   • Myotonic dystrophy type 2 typically presents in adulthood and has variable manifestations such as early onset cataracts (less than 50 years of age), various grip myotonias, thigh muscle stiffness, muscle pain, and weakness (in hip flexors, hip extensors, or long flexors of the fingers) 4-6, 14, 64-67.

   Myotonic dystrophy type 2: the 2020 update - PMC - National Center for

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3. my.clevelandclinic.org › health › diseasesMyotonic Dystrophy: What It Is, Symptoms, Types & Treatment

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   Symptoms of myotonic dystrophy type 2. Symptoms of myotonic dystrophy type 2 (DM2) typically begin in adulthood and can vary. Symptoms can include: Proximal muscle (the muscles closer to the center of your body) weakness or stiffness. Myofascial pain. Early-onset cataracts (occurring before the age of 50). Varying grip myotonia. Hearing loss.

4. www.medicalnewstoday.com › articles › myotonic-dystrophyMyotonic dystrophy: Types, causes, symptoms, treatments

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   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 relaxing their muscles....

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6. www.webmd.com › brain › myotonic-dystrophy-overviewMyotonic Dystrophy: Types, Symptoms, Causes, and Treatment

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   Apr 13, 2022 · With the congenital form, people may have weak muscle tone, breathing problems, clubfoot (an inward and upward turning of their foot ), intellectual disability, or delayed development. Some of...

7. www.ncbi.nlm.nih.gov › pmc › articlesMyotonic dystrophy type 2: the 2020 update - PMC

   www.ncbi.nlm.nih.gov › pmc › articles

   Dec 1, 2020 · Myotonic dystrophy type 2 typically presents in adulthood and has variable manifestations such as early onset cataracts (less than 50 years of age), various grip myotonias, thigh muscle stiffness, muscle pain, and weakness (in hip flexors, hip extensors, or long flexors of the fingers) 4-6,14,64-67. These complaints often appear between 20 and ...

   • Author: Giovanni Meola
   • DOI: 10.36185/2532-1900-026

   • Publish Year: 2020
   • Publication: Acta Myol. 2020 Dec; 39(4): 222-234.

8. www.verywellhealth.com › myotonic-muscularMyotonic Muscular Dystrophy: Symptoms and Prognosis

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   Apr 9, 2024 · What Are the Symptoms of Myotonic Muscular Dystrophy? The symptoms of myotonic muscular dystrophy can begin at any age between infancy and the age of 40. If you or your child has DM 1 or DM 2, you may experience some of the following. Skeletal Muscle Weakness. Skeletal muscles are the voluntary muscles attached to your bones.

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     What is Myotonic Dystrophy Type II? - Gilbert Gottfried Passed Away After a Long Illness

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10. www.myotonicdystrophysupportgroup.org › myotonicMyotonic Dystrophy type 2 (DM2)

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    DM2 is an important diagnosis to consider in patients who have proximal muscle weakness around the shoulders and pelvis or a “limb-girdle weakness”. DM2 is an autosomal dominant genetic disorder which means that, on average, it is passed on to half of the children of an affected parent.

11. medlineplus.gov › condition › myotonic-dystrophyMyotonic dystrophy: MedlinePlus Genetics

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    Learn about the symptoms, causes, and inheritance of myotonic dystrophy, a group of inherited muscular disorders. Find out the differences between type 1 and type 2, and the variations of type 1.