Help Please I Can’t Find Any Answers Anywhere….?

Filed in Category Pediatric Specialists

One of my twin daughters was born with “extreme molding of the head” at 2 months they found that she no longer had a soft spot, but xrays showed no fusion of the sutures, they’ve been watching the growth of her head, at 2 mon. she was in the 90%, 3 mon. the 75% and now at 4 mon. shes barely in the 50%. The dr. says her head hasn’t grown since she was 2 mon. but another xray still showed no fusion of the sutures. We’re now waiting on the refferal for a pediatric neurosurgeon but if anyone has any ideas or information i’d reallly appreciate it. I don’t know if the xrays need to be read by a pediatric specialist in this area and maybe thats the problem, btu I can’t find any info. I don’t smoke or drink or do drugs and I never have I just say that to weed out any unneeded remarks. Please help if you can.

1 Comment so far

  1. NB on November 2, 2009 6:05 pm

    Hello, my son (who is also a twin) had the same exact issue. His twin does not. I wanted to let you know that you are doing exactly what you are supposed to be doing! In my sons case they said he may need to have surgery to correct this issue. I was scared to death! His sutures showed no fusion as well. It is interesting to read your post because Joshua’s percentlile kept dropping at every visit…the same as your daughters did. The doctors were suspecting craniostenosis. It is when the head is not growing due to the sutures closing prematurly.They have sites on the web devoted to this I will list some below for you. We went and saw a Nuero surgeon at Cedars Sanai in Southern California he said he wanted to wait and see what happens, Since his head still “fit” his little frame. Well here we are and Joshua is now 3 and a half. He is still a little guy and his head is still on the small side, still in the 40% however he never needed surgery. We found out at 6 months that he has a genetic condition that is known to cause this sort of problem along with numerous others. It is called 22q deletion syndrome, a piece of his chromosome #22 is missing. Has she had any genetic testing done to rule out other issues? I dont want to freak you out more (lord knows your heart cant take it) but I did want to tell you from a mother who has been exactly in your shoes … that way you had some hope. We dont see any future head issues as far as growth goes due to the fact that his head is still growing REALLY SLOWLY! but so is his body. I will be wishing for the best for you and your family good luck!!http://cpmcnet.columbia.edu/dept/nsg/PNS…http://en.wikipedia.org/wiki/Craniosynos…





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