Does anybody know about Emery-Dreifuss muscular dystrophy?

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If me and my boyfriend were to have a kid, I need to know what would happen. He has Emery-Dreifuss muscular dystrophy. The doctors explained it to him, but hes sleeping and I really want to know right now. Is there a way to have a child naturally without the child getting it? Or is invetro the only way? Thank you!
Genetic counseling is advised when there is a family history of muscular dystrophy. Women may have no symptoms but still carry the gene for the disorder. Duchenne muscular dystrophy can be detected with about 95% accuracy by genetic studies performed during pregnancy.
Only males are affected clinically by X-linked inheritance. Genes associated with Emery-Dreifuss dystrophy encode for the nuclear membrane proteins lamin A/C (autosomal) and emerin (X-linked).  (+ info)

I am doing a research paper on Emery-Dreifuss Muscular Dystrophy (EDMD) and I need some help??? Please help?

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I am doing a research paper on EDMD. It's practically on a person with EDMD's daily life. I am having trouble finding a few of the facts for my project.
I need to know:

-descriptive words to descirbe his/her personality
-family life of person
-Major Hardships for character


A list of websites would also be helpful :)
thanks
http://www.healthline.com/galecontent/emery-dreifuss-muscular-dystrophy, pls try this website  (+ info)

Muscular dystrophy?

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Hello all.
I'm ashley and I'm teaching my fellow AP biology classmate about muscular dystrophy. I would like to be able to tell them how someone who has Muscular dystrophy deals with it in their daily lives. I would be happy to hear anything you have to say.
Thank you,
Ashley
Ashley, you can try webmd.com, mayoclinic.com, familydoctor.org for some disease information and hopefully these websites will also have some links on support groups as well, good luck  (+ info)

Muscular Dystrophy...?

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My friend is dating a guy who has muscular dystrophy and she's wondering if her future children (if she has any with him) will have the disease. Fact-filled answers would be much appreciated. Thanks. :]
well, muscular dystrophy is a recessive, and in some cases, X-linked trait, meaning that the trait for muscular dystrophy is on the X chromosome (females have two x choms, males have an x and a y). Basically, any son she had would have at least a 50% chance of having the disease, and depending on whether she is a carrier for the trait (meaning that she carries the trait for muscular dystrophy, but doesn't show it because it is recessive), her daughters would either have a 0% chance of having it (if your friend isn't a carrier) or a 50% chance of having it (if she is a carrier). a good way for her to get some idea on wheather or not she's a carrier, she can look back at her family history and see if any distant family members have shown the trait for Muscular dystrophy.

Hope this helps  (+ info)

Muscular dystrophy disease?

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what is the genetic history of emery dreifuss muscular dystrophy, and what are the chances of a person to get it?
thnx
I know that both parents have to carry the gene for MD.  (+ info)

How long will muscular dystrophy telethon go on?

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Doesn't most muscular dystrophy patients have insurance?

I would think if they are poor they would have medicaid.

So, are most of the money made during the telethon go to research?

Not making much progress are they? I think they've been doing the telethon for over 30 years at least.

I think it's a scam.
It will be on for 24 hours.  (+ info)

Where does duchenne muscular dystrophy strike most?

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I need information on duchenne muscular dystrophy, where does it strike most? Like, what part of the body does it affect the most? What new information from scientists is there that has to do with duchenne muscular dystrophy? How far are they in the research?
Duchenne muscular dystrophy (DMD) is a severe recessive X-linked form of muscular dystrophy characterized by rapid progression of muscle degeneration, eventually leading to loss of ambulation and death. This affliction affects one in 3500 males, making it the most prevalent of muscular dystrophies. In general, only males are afflicted, though females can be carriers. Females may be afflicted if the father is afflicted and the mother is also a carrier/ affected. The disorder is caused by a mutation in the gene DMD, located in humans on the X chromosome (Xp21). The DMD gene codes for the protein dystrophin, an important structural component within muscle tissue. Dystrophin provides structural stability to the dystroglycan complex (DGC), located on the cell membrane.

Symptoms usually appear in male children before age 5 and may be visible in early infancy. Progressive proximal muscle weakness of the legs and pelvis associated with a loss of muscle mass is observed first. Eventually this weakness spreads to the arms, neck, and other areas. Early signs may include pseudohypertrophy (enlargement of calf and deltoid muscles), low endurance, and difficulties in standing unaided or inability to ascend staircases. As the condition progresses, muscle tissue experiences wasting and is eventually replaced by fat and fibrotic tissue (fibrosis). By age 10, braces may be required to aid in walking but most patients are wheelchair dependent by age 12. Later symptoms may include abnormal bone development that lead to skeletal deformities, including curvature of the spine. Due to progressive deterioration of muscle, loss of movement occurs eventually leading to paralysis. Intellectual impairment may or may not be present but if present, does not progressively worsen as the child ages. The average life expectancy for patients afflicted with DMD varies from late teens to early to mid 20s. There have been reports of a few DMD patients surviving to the age of 40, but this is extremely rare  (+ info)

What is the probability of a couple having a child with Muscular dystrophy if the mother is carrier?

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the mother is the carrier and the father unaffected. they have a son already with muscular dystrophy. another child is expected.
Duchenne Muscular Dystrophy (DMD), the most common form, is one of 9 types of muscular dystrophy. The sons of female carriers each have a 50% chance of having the disease. The daughters of female carriers each have a 50% chance of becoming carriers themselves but will not have the disease if the gene is linked to DMD. But since you haven't stated which type of dystrophy the existing son has, I'm not able to work with complete information and I'm going on the assumption that the child has DMD.  (+ info)

What should i do for my muscular dystrophy presentation?

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For school we have to do a presentation on muscular dystrophy. I made a powerpoint but my teacher said I need something else that is more creative.... Any Ideas???
  (+ info)

Does anybody have photos of people with Muscular Dystrophy?

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I am doing a powerpoint of Muscular Dystrophy for my College kine course. The purpose of my presentation is to inform people about Muscular Dystrophy. I picked the subject because I have Muscular Dystrophy as well and feel that people must know what it is and the different types.
here you go!


http://images.google.com/images?hl=en&safe=off&rlz=1G1GGLQ_ENUS293&um=1&ei=mnEAS7a7GJ2UtgOV29SeCg&sa=X&oi=spell&resnum=0&ct=result&cd=1&q=muscular+dystrophy&spell=1&start=0  (+ info)

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