Your questions seems to be aimed at the MEdhelp audience
When the corpus callosum is missing, this is termed 'agenesis of the corpus callosum' and is a feature of several developmental brain problems including for instance Arnold-Chiari type II and Aicardi syndrome. Sometimes it can just occur on its own, and subarachnoid cysts are relatively common on their own as well.
Early intervention with special ed and other support services are important to maximise any potential a child with these problems has and can make a big difference. As long as you are doing this, at least you know you are doing everything, and you have to let him reach his own potential.
One might condsider doing an EEG to look for subtle seizures if there is a concern about him not doing as well as he should for his own baseline.
Cindy I also have cyst and HYDRO. My first 50 years were fine, cognitive and really quite normal. Special education was not required,the last 10 years have been a continious decline both physical and mental.I had to retire because of short term memory problems. The only advice for you is have a lot of patience with your son. He will have to deal with peer pressuure pressure himself. Best wishes to both and always display a positive attitude.
This is new to me. Was diagnosed with what they think is an anarachnoid cyst the end of last year. They found it while doing different tests for my cervical disc fusion, which did not take place. My neurologist told me he wasn't sure if it was a cyst, or just fluid collecting and that was it. He said it was nothing to worry about. Had surgery 12/21/05 for a redo on my disc fusion that didn't fuse (posterior) but now am experiencing weird head pressure coming from my incision in the back of neck to the top of my head. Exactly what are the symptoms of an arachnoid cyst with hydrocephalus? was wondering if this is from my neck surgery or from what they think is the cyst.
I'm a 35 year old female that was told that I have a arachnoid cyst on or at the midline of the posterior fossa.I have so many things going on and would like to know if someone can tell me if the related to the cyst.I have lost the feeling in my hands and feet my legs on occasion,my head feels so heavy and the headaches are worst than a migraine.I get hotflashes,mood swings,and the back of my kneck swells as well as my back.my vision gets blurry and I have now noticed that I am begining to have some hearing loss in the right ear.I feel like I have heat in my head at times as if someone had lite a match in there.The cyst as of august 2004 was only 2.2x3cm and I have not gotten it checked since due to going to 2 doctors that say there is nothing they can do but pain management so I do not know if it has grown since then.please help understand this thing in my head and if these are symptoms of the cyst.
I was also born with a subarachnoid cyst and partial agenesis of the corpus callosum. I can't tell the difference in severity between your son's case and mine, so take this for what it's worth. I had a lot of difficulty in school, for various reasons. I was shorter than most of the people in school for quite a few years due to pituitary gland problems, but I also have learning disabilities. I'd actually say that most of my time in school was pretty miserable, but that was just because of a lack of understanding on the part of my teachers and parents. I finally went in for a full psychological study and was told that I am extremely intelligent, and that there are medical proofs to back up what I'd been trying to say about my difficulties in memory loss and learning.
The best advice that I can give is to try to be patient and understanding with your son, and above all, do anything you can to educate his teachers and yourself about the learning difficulties that he is facing. I can remember being lectured about being lazy because they couldn't believe that I actually did the homework but just forgot it at home. Reassure your son that his problems in learning have nothing to do with his intelligence. What I've learned to do in my case is to try to find ways to compensate for my memory. If I have a list of things to do, I know now that it all has to be written down for it all to get done. I hope that helps. I won't go into too much detail here, so it won't get long, but if you need to talk more about this, feel free to email me at Blake.***@****. Good luck! :)