Dystrophy Sentence Examples

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

Garry, a mature student at Queen's Armagh campus, has dystrophy.

It is reported to be due to congenital muscular dystrophy.

Peter French, who suffers from muscular dystrophy, was looking forward to starting at Luton Sixth Form College last month.

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

Confusion often arises over the use of the term " corneal dystrophy " in dogs.

The group have studied a number of conditions associated with progressive retinal dystrophy.

Dean has a rare condition known as rod and cone dystrophy, which he's had since the age of nine.

We both felt that Jessica could not possibly have muscular dystrophy.

Duchenne muscular dystrophy is not treated by bracing.

However, muscular dystrophy (technically a myopathy) is far more severe.

Some types of muscular dystrophy are fatal in early adulthood.

Symptoms of muscular dystrophy (MD) diseases usually appear during childhood and adolescence.

The forms of muscular dystrophy differ according to the way they are inherited, the age at which symptoms begin, the muscles they affect, and how fast they progress.

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

Muscular dystrophy is generally a more serious disease than many other types of myopathies.

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

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

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

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

Myotonic dystrophy has an effect called "anticipation."

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

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

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

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

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

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

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

Muscular Dystrophy Association [cited October 9, 2004].

By 1997, approximately 800 different diagnostic tests were available, most of them for hereditary genetic disorders such as Tay-Sachs disease, sickle cell anemia, hemophilia, muscular dystrophy, and cystic fibrosis.

Muscular dystrophy is the name for a group of inherited disorders in which strength and muscle bulk gradually decline.

Duchenne muscular dystrophy (DMD), which affects young boys, causing progressive muscle weakness, usually beginning in the legs.

It is the most severe form of muscular dystrophy.

Limb-girdle muscular dystrophy (LGMD), which begins in late childhood to early adulthood and affects both men and women, causing weakness in the muscles around the hips and shoulders.

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.

Congenital muscular dystrophy (CMD), which is present from birth, results in generalized weakness, and usually progresses slowly.

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

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

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.

New mutations are less common in other forms of muscular dystrophy.

A boy with Duchenne muscular dystrophy usually begins to show symptoms as a preschooler.

This type of muscular dystrophy usually begins in early childhood, often with contractures preceding muscle weakness.

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

A person with this dystrophy has difficulty relaxing his grasp, especially if the object is cold.

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

Severe disability affects most people with this type of dystrophy within 20 years of onset, although most do not require a wheelchair even late in life.

Diagnosis of muscular dystrophy involves a careful medical history and a thorough physical exam to determine the distribution of symptoms and to rule out other causes.

Changes in the structure of muscle cells and presence of fibrous tissue or other aberrant structures are characteristic of different forms of muscular dystrophy.

Decreased response is seen in muscular dystrophy.

For most forms of muscular dystrophy, accurate diagnosis is not difficult when done by someone familiar with the range of diseases.

Treatment of muscular dystrophy is mainly directed at preventing the complications of weakness, including decreased mobility and dexterity, contractures, scoliosis, heart defects, and respiratory insufficiency.

When any type of surgery is performed in people with muscular dystrophy, anesthesia must be carefully selected.

Most people with muscular dystrophy do not need a tracheostomy, although some may prefer it to continual use of a mask or mouthpiece.

Becker muscular dystrophy (BMD)-A type of muscular dystrophy that affects older boys and men and usually follows a milder course than Duchenne muscular dystrophy.

Distal muscular dystrophy (DD)-A form of muscular dystrophy that usually begins in middle age or later, causing weakness in the muscles of the feet and hands.

Duchenne muscular dystrophy (DMD)-The most severe form of muscular dystrophy, DMD usually affects young boys and causes progressive muscle weakness, usually beginning in the legs.

Both Duchenne muscular dystrophy and Becker muscular dystrophy are caused by flaws in the gene that tells the body how to make this protein.

Limb-girdle muscular dystrophy (LGMD)-A form of muscular dystrophy that begins in late childhood to early adulthood and affects both men and women.

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

Oculopharyngeal muscular dystrophy-A type of muscular dystrophy that affects adults of both sexes, causing weakness in the eye muscles and throat.

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.

There is no known link between nutrition and the onset of muscular dystrophy.

Prospective parents with first-degree relatives (parents, siblings, or other children) who have been diagnosed with muscular dystrophy should consider including counseling in their family planning process.

These include cystic fibrosis, asthma, cerebral palsy, muscular dystrophy, and various immunodeficiency disorders.

He became a National Goodwill Ambassador for the Muscular Dystrophy Association and had the chance to meet Oprah Winfrey, Maya Angelou and Jimmy Carter to discuss his work and his hopes for peace in the world.

Health problems associated with external itchiness include vaginitis, vulvar dystrophy, Bartholin gland cyst, and diabetes.

Degenerative disorders like muscular dystrophy are difficult to detect at birth.

She has co-hosted a segment of the annual Jerry Lewis Telethon, which raises money and awareness for Muscular Dystrophy.

Sweeney has co-hosted the annual Jerry Lewis Labor Day Telethon to raise funds to fight Muscular Dystrophy three times, from 2007-2009.

One rare problem is called reflex sympathetic dystrophy or complex regional pain syndrome.

The work will develop fibers with optimal dimensions and solubility for cell growth do deliver genetically modified muscle cells to treat muscular dystrophy.

The mdx mouse is supposed to represent muscular dystrophy, but the muscles regenerate with no treatment.

He has muscular dystrophy and uses a wheelchair for mobility.

They can also develop bloat, elbow and hip dysplasia, or autosomal recessive muscular dystrophy.

This procedure is used to test for muscle disorders, including muscular dystrophy.

The most common causes of this type of scoliosis are cerebral palsy and muscular dystrophy.

Facioscapulohumeral muscular dystrophy (FSH), also known as Landouzy-Dejerine disease, which begins in late childhood to early adulthood and affects both men and women, causing weakness in the muscles of the face, shoulders, and upper arms.

About the same time, his calves will begin to swell, though with fibrous tissue rather than with muscle and feel firm and rubbery; this condition gives DMD one of its alternate names, pseudohypertrophic muscular dystrophy.