Talked to Julia today and just can't believe how amazing she is! She took over half a hour of her time today to talk to me. Thanks Julia and thanks to Cherubs for giving me this opportunity!
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Talked to Julia today and just can't believe how amazing she is! She took over half a hour of her time today to talk to me. Thanks Julia and thanks to Cherubs for giving me this opportunity!
Amanda Mother of Liz born 09/09/2002 with LCDH,Emily 05/27/2005. Liz was diagnosed at 12 weeks in uetro 90 percent of left diaphragm missing. Gortex patch put in at 3 days old. Ever abdominal organ other then kidneys herniated. Born at 38 weeks, 6 lbs 11oz. Born in Hamilton ON. Hospitalized for 6 weeks. Rehirniated at age 6 and 3 surgeries age 10 almost lost my Cherub again. Duplication cysts on her stomach. Reflux and on going GI issues.
Mandy,
I think I missed your question last week. I'm sorry for my late reply.
We have seen a region of chromosome 17 called 17q12 deleted (missing) in children with CDH. We have not seen this region duplicated (extra) in children with CDH. This region of chromosome 17 is one or the more common chromosome microdeletion (missing) or microdupliation (extra) we see in children. Most children with this region deleted or duplicated don't have a CDH. The more common symptoms are developmental delay and learning problems. Some individuals have no symptoms of the deletion.
This shows how complex genetics is and particularly this portion of chromosome 17.
Please feel free to email me with more specific question to jw2500@columbia.edu.
Best,
Julia
The DHREAMS study is an NIH funded multicenter national research study of congenital diaphragmatic hernia (CDH). The goal of our study is to improve the understanding of the causes of CDH. http://www.cdhgenetics.com/
Jess,
Congratulations on your baby girl. I hope she is doing well.
You are correct that Right is less common than Left. We are not exactly sure why that is but we think it has to do with how the three sheets of muscle come together to form the diaphragm in early fetal development. This convergence of the muscles is more often disrupted on the left side.
We also have seen that children with a Right sided do not necessarily have a worse prognosis but may need more intervention than children with a Left sided hernia. In our follow up of 250 children with a CDH, we found that children with a Right sided CDH needed ECMO more often than L sided CDH but did not over all have a worse outcome than children with a Left sided CDH.
We have seen families with members with both Left sided and Right sided CDHs which leads us to believe that at least some of the genetic causes are the same but we also suspect that some genetic causes only cause a Right sided CDH and some only cause a Left sided CDH. We are working to answer all of these questions.
Best,
Julia
The DHREAMS study is an NIH funded multicenter national research study of congenital diaphragmatic hernia (CDH). The goal of our study is to improve the understanding of the causes of CDH. http://www.cdhgenetics.com/
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