Member Comments are provided by individuals and reflect their personal opinions only. Under NO circumstances should you act on any advice or opinion posted in this forum.  ALWAYS check with your personal physician before taking any action regarding your health! MedHelp International and our partners, sponsors and affiliates have no obligation to monitor any comments posted on this site, or the content and/or accuracy of such exchanges. MedHelp International does not endorse the views of any user.
Neurology  (Expert Forum)
 | 
Arnold Keari Type 1
This forum is for questions and support regarding neurology issues such as: Alzheimer's Disease, ALS, Autism, Brain Cancer, Cerebral Palsy, Chronic Pain, Epilepsy, Fibromyalgia, Headaches, MS, Neuralgia, Neuropathy, Parkinson's Disease, RSD, Sleep Disorders, Stroke, Traumatic Brain Injury

Arnold Keari Type 1

by lori, May 12, 2000 12:00AM
My son, one of triplets, just had a brain MRI done on Wednesday. My husband and I met with our pediatrician who said that J. has a rare brain abnormaility called Arnold Keari Type 1.  She was unable to give us much information since she said that after looking through medical books and on line that she was not able to find much to inform us on.  We will be meeting with a neuro-surgeon on Wed. May 17 and I am very interested in asking the most appropriate questions.  I am also interested in any sites, journals and/or resources that are available to further educate myself on this disorder.  Please help!!!! thank you - lori

by CCF Neuro[P] MD, RPS, May 12, 2000 12:00AM
Dear Lori:



The Arnold Chiari malformation is extremely serious as it includes a spina bifida (hole in the spinal column that communicates to the skin, the depression of the cerebellum and brainstem into the spinal column, and usually hydrocephalus.  Is this being diagnosed in utero?  There are currently some centers doing in utero surgeries for this conditions and this may lead to a better prognosis.



If you triplets are already born, and there is no spina bifida, then likely you misunderstood and this is a Chiari I malformation.  This is not that uncommon, and when it is mild, there are usually no, NO, NO, NO neurological consequences.  Sometimes when it is large, it can cause problems and surgery is warranted (respiration problems, intermittent hydrocephalus).  I would wait and see the neurosurgeon or your pediatric neurologist before worrying.  Most likely, in the face of a normal triplet baby, I would think it will turn out to be a minor Chiari I.



Sincerely,



CCF Neuro MD
Member Comments (7)

by lori, May 14, 2000 12:00AM
thank you for your reply regarding Arnold Chiari malformation.  we will be seeing a neuro surgeon on this coming wednesday.  can you advise me of any specific questions i should ask about.  my first question was in regards to a thinning cerebral cortex which is totally unrelated to this malformation.  could you give me some additional information on what i could possibly expect from this .  thank you - lori

by CCF Neuro[P] MD, RPS, May 14, 2000 12:00AM
Dear Lori:



As previously mentioned, there is no such entity as an Arnold Chiari I malformation.  So, you need to clarify the diagnosis.  Second, if your son has a Arnold Chiari, you need to ask questions concerning the meningomyelocele in his back.  Since your diagnosis is uncertain, I would have him/her have the neuroradiologist review the MRI scan.



CCF Neuro MD

by lori, May 15, 2000 12:00AM
I am sorry that I have been giving you the wrong information.  J. has Arnold Chiari Type 1, not Arnold Chiari 1 as I have been mistakingly typing.  Does this change any thing now as far as your responses go? thank you for all of your help. It really appreciate your quick responses.

by CCF Neuro[P] MD, RPS, May 15, 2000 12:00AM
Dear Lori:



Again, there is not such thing as an Arnold Chiari I, it is either Chiari I or Chiari II or Chiari III malformation.  An Arnold Chiari malformation is a Chiari II malformation.



CCF Neuro MD

by Eric, Jul 13, 2000 12:00AM
this proves even doctors can be anal. they knew what the mother saying but put her in hell to answer it. then the doctor say the chiari malformation type 1 does not cause problem. how would they know they have never had chiari type 1.



thank you, thank you

by Rocky, Jul 15, 2000 12:00AM
Hope you have have had some positive results since your initial

questions regarding your child.  Although I am not a medical

expert, I could be called a well-traveled patient.  The good

news is that a surgical procedure may be available for your child's condition.  However, it would be advisable to find a

neurosurgeon who is very familiar with Chiari Malformation

surgical procedures.  The down side to this is that, too often,

a neurologist's ego will not permit them to tell you that this is not their "area of specialization".

For more info on Chiari Malformation (otherwise known as Arnold-

Chiari}, Type I & II see http://cpmcnet.columbia.edu/dept/nsg/

PNS/ChiariMalformation.html
Continue discussion
Expert Activity
Coronary Artery Disease - Risk fact... updated
Aug 26 by Cleveland Clinic
"8 Drugs Doctors Would Never Take"
Aug 18 by Adam R. Tanase, D.C.
Elevated Choleterol 101-who needs t... 
Aug 13 by Lee Kirksey, MD