Myotonic sentence example

myotonic
  • The mechanism of other dominant mutations such as the one that causes myotonic dystrophy is not yet known.

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  • When the DNA was switched on the mice showed all the symptoms of myotonic dystrophy.

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  • Other more common types of MD are Becker's, myotonic dystrophy, limb-girdle MD, and facioscapulohumeral MD. MD is more common in boys.

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  • Myotonic dystrophy is a progressive disease in which the muscles are weak and slow to relax after contraction.

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  • Myotonic dystrophy (DM), also called dystrophia myotonica, myotonia atrophica, or Steinert disease, is a common form of muscular dystrophy.

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  • Myotonic dystrophy is an uncommon disease occurring in about one out of every 8,000 individuals.

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  • The most common type of DM is called DM1, which is caused by a mutation in a gene called myotonic dystrophy protein kinase (DMPK).

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  • Myotonic dystrophy has an effect called "anticipation."

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  • Having repeat numbers greater than 1,000 causes congenital myotonic dystrophy.

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  • This genetic defect is called DM2 or proximal myotonic myopathia (PROMM).

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  • In general, myotonic dystrophy causes weakness and delayed muscle relaxation called myotonia.

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  • The most severe form of DM, congenital myotonic dystrophy, may appear in newborns of mothers who have DM1.

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  • Congenital myotonic dystrophy is marked by severe weakness, poor sucking and swallowing responses, respiratory difficulty, delayed motor development, and mental retardation.

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  • Most people with myotonic dystrophy maintain the ability to walk, even late in life.

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  • It is not unusual for a woman to be diagnosed with DM after she has an infant with congenital myotonic dystrophy.

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  • Myotonic dystrophy cannot be cured, and no treatment can delay its progression.

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  • Myotonic dystrophy, also known as Steinert's disease, which affects both men and women, causing generalized weakness first seen in the face, feet, and hands.

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  • Myotonic dystrophy is the most common form of muscular dystrophy, affecting more than 30,000 people in the United States.

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  • Myotonic dystrophy is linked to gene defects for a protein that may control the flow of charged particles within muscle cells.

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  • It is possible that this mutation affects nearby genes as well, and that the widespread symptoms of myotonic dystrophy are due to a range of genetic disruptions.

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  • Symptoms of myotonic dystrophy include facial weakness and a slack jaw, drooping eyelids (ptosis), and muscle wasting in the forearms and calves.

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  • Myotonic dystrophy affects heart muscle, causing arrhythmias and heart block, and the muscles of the digestive system, leading to motility disorders and constipation.

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  • Myotonic dystrophy-A form of muscular dystrophy, also known as Steinert's disease, that affects both men and women.

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  • People with dystrophies with significant heart involvement (BMD, EDMD, Myotonic dystrophy) may nonetheless have almost normal life spans, provided that cardiac complications are monitored and treated aggressively.

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