Cmt sentence example
Details of past projects of the CMT using the old micrometer can be found here.
The show is set to premiere in January 2008 on CMT, Country Music Television.
After listening to the backlash and public outcries about his decision for days, John Rich posted an explanation "Why I Picked Julio as the Winner" on the CMT website.
Rich was the host of CMT's Gone Country, a show similar to Nashville Star but featuring celebrities as opposed to unknown contestants.
Whether you can't live without CMT or just know a good song when you hear it, country music can become a big part of your life.Advertisement
Charcot-Marie-Tooth disease (CMT) is the name of a group of inherited disorders of the nerves in the peripheral nervous system.
The age of onset of CMT can vary anywhere from young childhood to the 50s or 60s.
Although CMT has been described for many years, it is only since the early 1990s that the genetic cause of many of the types of CMT have become known.
Therefore, knowledge about CMT increased dramatically shortly thereafter.
Therefore, people with CMT also have sensory loss.Advertisement
There are two parts of the nerve that can be affected in CMT.
Children who have problems with the myelin have CMT type 1 and children who have abnormalities of the axon have CMT type 2.
There are probably at least 15 different genes that can cause CMT.
The most common type of CMT, called CMT1A, is caused by a mutation in a gene called peripheral myelin protein 22 (PMP22) located on chromosome 17.
In most people who have CMT, the mutation that causes the condition is a duplication (doubling) of the PMP22 gene.Advertisement
People who have HNPP may have some of the signs of CMT.
Another type of CMT, called CMT1B, is caused by a mutation in a gene called myelin protein zero (MPZ), located on chromosome 1.
Another type of CMT, called CMTX, is usually considered a subtype of CMT1 because it affects the myelin, but it has a different type of inheritance than type 1 or type 2.
There are at least five different genes that can cause CMT type 2.
Because it has just been discovered, not much is known about how mutations in this gene cause CMT.Advertisement
This is a severe type of CMT in which symptoms begin in infancy or early childhood.
It is known as of 2004 that this is not a separate type of CMT; in fact, people who have onset in infancy or early childhood often have mutations in the PMP22 or MPZ genes.
Children with type 3 CMT may not develop early motor skills such as walking until they are three or four years old.
More research is required to understand how mutations in these genes cause CMT.
Children with CMT have an increased risk for passing on the genes that cause the condition when they start a family of their own.Advertisement
Therefore, individuals who have these types have a 50 percent, or one in two, chance of passing CMT on to each of their children.
Thus, when a male has a mutation in his Cx32 gene, he will have CMT.
If they have a mutation in one copy of their Cx32 genes, they will only have mild to moderate symptoms of CMT that may go unnoticed.
If a woman with a Cx32 mutation passes her normal X chromosome, she will have an unaffected son or daughter who will not pass CMT on to his or her children.
Two carrier parents have a 25 percent, or one in four, chance of passing CMT on to each of their children.
The main problems caused by CMT are weakness and loss of sensation mainly in the feet and hands.
Most children with CMT remain able to walk throughout their lives.
When CMT is suspected in a child, the diagnosis begins with a careful neurological exam to determine the extent and distribution of weakness.
This test may show characteristic features of CMT, but it is not diagnostic of CMT.
A nerve biopsy (removal of a small piece of the nerve) may be performed to look for changes characteristic of CMT.
However, this testing is not diagnostic of CMT and is usually not necessary for making a diagnosis.
Definitive diagnosis of CMT is made only by genetic testing, usually performed by drawing a small amount of blood.
All affected members of a family have the same type of CMT.
Therefore, once a mutation is found in one affected member, it is possible to test other members who may have symptoms or are at risk of developing CMT.
However, physical and occupational therapy are an important part of CMT treatment.
It is very important that individuals with CMT avoid injury that causes them to be immobile for long periods of time.
It is often difficult for people with CMT to return to their original strength after injury.
Complete lists are available from the CMT support groups.
Parents considering providing any of these medications to their children with CMT should weigh the risks and benefits with their physician.
The symptoms of CMT usually progress slowly over many years but do not usually shorten life expectancy.
The majority of children with CMT do not need to use a wheelchair at any time during their lives.
Most people with CMT are able to lead full and productive lives despite their physical challenges.
As of 2004 there was no known way to prevent CMT.
Genetic counseling for parents with CMT can help them understand the risk they face of having children with the disorder.
The goal for children with CMT is to live as normal a life as possible.
Learning about CMT and discussing it with teachers, classmates, friends, and family members may help normalize the disorder and create support for the child.
Similar television stations followed, such as VH-1, The Box, MTV2, Fuse and CMT (Country Music Television).
Country Music Countdown - This chart compiled by Country Music Television (CMT) includes video plays in the calculations of their charts.
My Big Redneck Wedding is a reality TV show that airs on CMT.
It wasn't until February 27, 2008, that Fox announced it had sold the rights to Trading Spouses to CMT, effectively ending the series.
As of September 2009, Trading Spouses reruns still appear on CMT.
He also competed on CMT's reality show Gone Country, which challenged musician from other genres to play country music and win the release of their own country single.