dm2 | Myotonic Dystrophy type 2 (DM2)

Keyword	CPC	PCC	Volume	Score	Length of keyword
dm2	1.58	0.5	8546	86	3

Keyword	CPC	PCC	Volume	Score
dm2	1.04	0.5	6086	37
dm2 icd 10	0.78	0.9	1854	62
dm2 medical abbreviation	0.22	0.8	439	11
dm200 digital mailing system	0.12	1	5924	15
dm247	0.03	0.8	2617	42
dm200	1.53	0.1	6568	30
dm23	0.16	1	1719	99
dm295	1.78	0.2	7171	7
dm2 to m2	0.93	0.6	3015	80
dm21	1.72	0.1	5944	76
dm250	1.5	0.6	7986	82
dm2 to cm2	1.02	0.5	3016	61
dm220	0.09	0.2	8790	78
dm2 with hyperglycemia icd 10	0.59	0.1	3224	82
dm2652rbx	0.4	0.2	1832	73
dm280	0.38	0.7	2770	50
dm2 with neuropathy icd 10	1.34	0.5	367	38
dm2 penndot	0.41	0.5	1444	71
dm200d	1.17	0.3	7433	59
dm250x	1.73	0.4	6912	7
dm2c-lp	1.36	0.5	1156	93
dm2 icd 10 code	0.13	0.5	1156	48
dm2 with ckd icd 10	0.51	0.6	7738	45
dm2 to mm2	0.92	0.9	4396	30
dm2 medications	0.91	1	7041	55

Search Results related to dm2 on Search Engine

Myotonic Dystrophy type 2 (DM2)
myotonicdystrophysupportgroup.org

https://www.myotonicdystrophysupportgroup.org/myotonic-dystrophy-type-2-dm2/

WEBDM2 is a multi-system disorder characterised by an inability to relax muscles once they have contracted or “myotonia” and muscle weakness. DM2 is generally a milder condition than DM1.The clinical onset of DM2 is typically in the third or fourth decade, with the most commonly presented symptoms being muscle weakness, stiffness and pain.

DA: 1 PA: 72 MOZ Rank: 51

Signs and Symptoms of Adult-Onset DM1 and DM2 - Myotonic Dystrophy (DM
mda.org

https://www.mda.org/disease/myotonic-dystrophy/signs-and-symptoms/adult-onset-DM

WEBOnset for DM2 ranges from the second to the seventh decade of life, often presenting with myotonia, weakness, or cataracts. In general, DM2 is a less severe disease than classic DM1. In most cases, weakness predominantly involves the proximal muscles, particularly the hip girdle muscles. 2

DA: 1 PA: 28 MOZ Rank: 14

Myotonic Dystrophy: What It Is, Symptoms, Types & Treatment
clevelandclinic.org

https://my.clevelandclinic.org/health/diseases/24516-myotonic-dystrophy-dm

WEBSymptoms 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. Pain is one of the primary complaints in ...

DA: 51 PA: 84 MOZ Rank: 49

Myotonic Dystrophy Type 2 - GeneReviews® - NCBI Bookshelf
nih.gov

https://www.ncbi.nlm.nih.gov/books/NBK1466/

WEBSep 21, 2006 · 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.

DA: 38 PA: 70 MOZ Rank: 50

Myotonic Dystrophy (DM) - Muscular Dystrophy Association
mda.org

https://www.mda.org/disease/myotonic-dystrophy/types

WEBMyotonic dystrophy (DM) includes two major types — DM1 and DM2 — both caused by genetic defects. They result in multisystem disorders characterized by skeletal muscle weakness and myotonia (difficulty relaxing muscles after use), cardiac abnormalities, cataracts, and other abnormalities.

DA: 26 PA: 63 MOZ Rank: 38

Causes/Inheritance - Myotonic Dystrophy (DM) - Diseases
mda.org

https://www.mda.org/disease/myotonic-dystrophy/causes-inheritance

WEBType 1 myotonic dystrophy (DM1) and type 2 myotonic dystrophy (DM2) are both caused by abnormally expanded stretches of DNA. The expansions occur in two different genes but appear to have similar effects on various cells, particularly the cells of the voluntary and involuntary muscles, including the heart and nervous system.

DA: 60 PA: 39 MOZ Rank: 60

Myotonic dystrophy type 2: the 2020 update - PMC - National …
nih.gov

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7783423/

WEBDec 1, 2020 · The myotonic dystrophies are the more frequent muscle disorders in adulthood. So far 2 distinct entities have been described: myotonic dystrophy type 1 (DM1) and myotonic dystrophy type 2 (DM2). In this article I review the discovery of the gene, the clinical features, pathogenetic and management of more recently described DM2.

DA: 36 PA: 77 MOZ Rank: 84

DM2 | Myotonic Dystrophy Foundation
myotonic.org

https://www.myotonic.org/dm2

WEBMar 20, 2024 · DM2. Myotonic dystrophy type 2, also known as proximal myotonic myopathy (PROMM), is a milder form of myotonic dystrophy in which transient muscle pain is the most common complaint. Only adult-onset forms of DM2 have been recognized.

DA: 81 PA: 66 MOZ Rank: 16

Myotonic Dystrophy Type 2: An Update on Clinical Aspects, …
nih.gov

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5240594/

WEBJul 7, 2015 · Myotonic dystrophy (DM) is the most common adult muscular dystrophy, characterized by autosomal dominant progressive myopathy, myotonia and multiorgan involvement. To date two distinct forms caused by similar mutations have been identified.

DA: 85 PA: 28 MOZ Rank: 68

Myotonic dystrophy - Wikipedia
wikipedia.org

https://en.wikipedia.org/wiki/Myotonic_dystrophy

WEBDM2. DM2 is generally milder than DM1, with generally fewer DM2 people requiring assistive devices than DM1 people. DM2 preferentially affects muscles closer to or on the torso, including the neck flexors, hip flexors, and hip extensors. Muscle pain is …

DA: 91 PA: 81 MOZ Rank: 81