MadSci Network: Genetics |
Hello Cindy. I'm sorry it's taken me so long to answer your question. I've looked into the inheritence patterns of CMT on the Mendelian inheritence in man website. http://www.ncbi.nlm.nih.gov/Omim/ This is the foremost web database for all of the genetic diseases identified to date. Unfortunately, for CMT, there are many different ways that the disease is transmitted and we can't be sure of what form of CMT your sons wife has. It looks like CMT can be transmitted either autosomal dominantly, autosomal recessively, or X-linked dominantly. The autosomal recessive form of CMT is the rarest. Also, according to the limited pedigree you gave for your daugter in law's parents, it would tend to rule out the autosomal recessive version of the disease. Should the disease be autosomal dominant in your daughter in law, then there would be a 50/50 chance of their child inheriting the disease, like you said. If it were an x-linked dominant, then it would also be a 50/50 chance for both a daughter or son. I would recommend you seek genetic counseling if you would really like a thorough analysis of the chances, since it's impossible to really analyze this with the limited pedigree you've given. Also, some of the genes involved in CMT disease are known, and it may be possible to test for mutations in your daughter in law that might let you all know exactly which CMT form she carries.
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