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Significats de myotonic dystrophy en anglès

portuguès
doença de steinert
espanyol
distrofia miotonica de steinert
català
distròfia miotònica de steinert
Wikidata

Long term genetic disorder that affects muscle function.

Termes relacionats
distròfia miotònica de steinert

A severe form of muscular dystrophy marked by generalized weakness and muscular wasting that affects the face and feet and hands and neck; difficult speech and difficulty with the hands that spreads to the arms and shoulders and legs and hips; the onset can be any time from birth to middle age and the progression is slow; inheritance is autosomal dominant.

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Examples for "dm1"
Examples for "dm1"
1
Conclusions: Patients with DM1 can develop rapid changes in cardiac conduction intervals.
Pubmed
2
Skeletal muscle, heart and smooth muscle are prominently affected in DM1.
Pubmed
3
The lifespans of the DM1 LBCLs were significantly shorter than normal cell lines.
Pubmed
4
Clinical findings in DM1 span a continuum from mild to severe.
Pubmed
5
Objective: We investigated care burden and its correlates among caregivers of patients with DM1.
Pubmed
1
The aim of our study is to assess the prognostic value of HRT in MD1 patients.
Pubmed
1
We present our experience with six patients affected by myxomatous degeneration associated to Steinert disease undergoing complex mitral valve repair.
Pubmed
Ús de myotonic dystrophy en anglès
1
Thornton said people with myotonic dystrophy have all the ingredients for a healthy body.
Reuters
2
Earlier collaboration has also resulted in an experimental drug for myotonic dystrophy that will soon begin development.
Reuters
3
Mice injected with a compound that neutralizes faulty gene activity regained the use of muscles frozen by myotonic dystrophy, the researchers said.
Reuters
4
We report a rare case of double heterozygous type I protein C deficiency and factor V Leiden in a patient with classic myotonic dystrophy.
Pubmed
5
These data indicate that muscle dysfunction is a core feature of SBMA caused by at least some of the same pathogenic mechanisms as myotonic dystrophy.
Pubmed