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Microcephaly: Rare Children's Disease Causes Small Head

Mental Retardation Due to Microcephaly

By Emma S., published Dec 07, 2005
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When my son was born he appeared so small, but at six pounds and nine ounces, he seemed perfectly healthy. That is, until I quickly discovered along with the physician, that he had no soft spot and his head was a little smaller than the average newborn. The attending physician quickly made arrangements to send my son to the Riley Children's Hospital in Indianapolis where he could be evaluated to determine if a skull problem was keeping the brain from growing or whether a developmental problem with the brain kept the skull from reaching normal proportions.

After many tests it was determined that my son had a condition called microcephaly. The condition is known by the small size of the head upon birth. With the condition, the brain fails to develop properly or stops growing completely, some time in the womb. The most frequent cause of the condition is genetic abnormalities that interfere with the development of the cerebral cortex, I was told.

Often associated with Down's syndrome, chromosomal syndromes or neurometabolic syndrome the condition can be caused by rubella, chicken pox, toxic chemicals, and drug or alcohol abuse. Although the actual reason for my son's abnormal head growth was never determined absolutely the results were the same as most microcephalic children: mental retardation.

Other conditions associated with microcephaly are speech and motor problems, facial distortions, dwarfism, hyperactivity, seizures, coordination and balance issues and other neurological problems. My own son's height reached 5', his head at 27 years is but 15" in circumference, he has frequent seizures, but no facial abnormalities. He can also do many things as if he were truly 27 years old, but turn around a few minutes later and act as if he's 4.

Takeaways
  • Children with microcephaly are often born without a soft spot.
  • Microcephalic children can have varying degrees of retardation - or none at all.
  • Disfigurement of the facial features is a common trait amongst kids with microcephaly.
Did You Know?
All people carry genes that, combined with the genes of another carrier, could cause a child to be born with microcephaly or another rare disease.
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My little girl was born with microcephaly, She changed my life in so many way, ( for the better). My little girl is definatly a gift from God. Her daddy and i gave her all the love we could possibly give, consequently she knows how to love and she definately knows how to show it. there are times when i don't remember her condition, the thruth is, at first it was difficult but as soon as you get a hang on it you'll realize it's not so bad. i would never change what God gave for nothing. God never gives more than what an induvidual can manage. There is just one problem i have and i know God will fix it for me. ( she constipate frequently).

Posted on 11/20/2008 at 10:11:55 AM

 
hiya.my brother was born with microcephaly and he is the best brother ever. Sure he is annoying and stupid sometimes but we still have a laugh and i jst because he is special needs dosent stop him from being him. I STRONGLY believe that Racheal 3 comments up should defently not terminate her prgenancy. Life is gods gift and you should love tht child no matter what. My brother dosent even act like he has anything wrong with him and he is just like an average human being and i love him very much. Remember, life is a gift!

Posted on 07/18/2008 at 10:07:45 AM

 
Never let anyone tell you to get rid of your child thats your decision to make not anyone else. Give that child a chance if you feel in your heart that its right. If you believe in god you know that he works miracles everyday and that child could be the greatest blessing in your life.

Posted on 06/12/2008 at 1:06:51 PM

 
Check out this blog...www.babybolte.blogspot.com. I have given birth to two babies with microcephaly....

Posted on 05/01/2008 at 12:05:32 PM

 
RACHAEL, I HAVE A 16 MONTH OLD W/ MICROCEPHALY. I ALSO FOUND OUT WHEN I WAS PREGNANT THAT I TOO WOULD BE FACING THIS RARE DEFORMITY. HAVING LOST A CHILD IN MY SECOND TRIMESTER PREVIOUS TO BECOMING PREGNANT W/ MY DAUGHTER. I WAS DEVESTATED. WHEN I GAVE BIRTH TO HER, SHE WAS DIAGNOSED W/ A MIRYAD OF OTHER PROBLEMS. I WAS TOLD AS SHE WAS SWEPT OFF TO THE NICU THAT IT WAS UNCERTAIN IF SURVIVAL WAS PROBABLE FOR HER. AT 4 DAYS OLD I TOOK HER TO A GENETIC DOCTOR WHO TOLD ME THEY COULD FIND NO REASON FOR HER TO HAVE THESE PROBLEMS, AND THAT AT 6 MOS OF AGE SHE WOULD BEGIN TO LOOSE HER HEARING AND EVENTUALLY HER SIGHT. MY DAUGHTER IS A HAPPY, HEALTHY, HEARING, LIVING CHILD. DO WHAT IS IN YOUR HEART. IF YOU TERMINATE, YOU WILL BE GIVING UP ON SOMETHING YOU HAVE BEEN CHOSEN TO HAVE. AND BELIEVE ME, IT IS TRULY A GIFT!

Posted on 04/29/2008 at 4:04:22 PM

 
Some of these stories made me cry! I have a beautiful baby girl just turned 9 months the microcephely was only diagnosed at birth however through pregnancy i had monitering every now and again. Charlotte was born via C Section and I was parted from her as she went in to a neonatel unit. She has Optic Nerve Hypoplasia and mild to moderate hearing loss. She is not sitting yet but lifting her head for prolonged periods of time. The genetesist told us today that she has (lissencephely) not sure of the spelling but this is what it sounded like but not on the worst end of the spectrum. Charlotte is just Charlotte and what she does and when she does it is up to her. I love her with all my heart no less no more than I would if she did not have her problems.

Posted on 04/09/2008 at 3:04:12 PM

 
I have a 10 yr old nephew with microcephley , they also said he wasnt going to walk or talk and he was going to be defromed... he is walking and gets his point across. he is our ANGEL and i feel so blessed that he chose my family to touch with his beautiful smile and loving compassionate soul.

Posted on 03/22/2008 at 8:03:42 PM

 
im 16 and i have an abnormally small head but the thing that confuses me is that im quite smarter than the average teen and no facial distorsions or whatever i dont knw if its a disformation of some kind or i migh have this microcephaly. i have no idea

Posted on 03/04/2008 at 2:03:54 PM

 
Gad bless you, have feith, trust him and things goes at the best it can be

Posted on 01/12/2008 at 9:01:50 PM

 
I HAVE A BEAUTIFUL LITTLE GRANDDAUGHTER WHO IS SEVERLEY DISABLED.SHE IS TWENTY MONTHS OLD. US SHE HAS MICROCEPHALY, A RARE HEART CONDITION,AND SHE IS TOTALLY BLIND.SHE CAN ONLY SEE LIGHT.A COUPLE OF MONTHS AGO SHE WAS DIAGNOSED WITH TYPE 1 DIABETES. HOW MUCH DOES ONE LITTLE SOUL HAVE TO ENDURE.SHE DOESN'T USE HER HANDS AT ALL,BUT SHE SUPRISED US ON CHRISTMAS DAY WHEN HER MUM PUT HER POSH OUTFIT ON AND WE ALL SAID SHE LOOKED BEAUTIFUL THE SMILE ON HER FACE WAS WORTH MORE THAN ANYTHING IN THE WORLD.LUCKILY WE CAPTURED HER ON VIDEO SHE ALSO MANAGED TO BANG ON HER DRUM. WHEN SHE WAS BORN WITH ALL THESE THINGS WRONG WITH HER I HAD HORRIBLE THOUGHTS THINKING SHE WOULD BE BETTER OFF DYING, HOW WRONG I WAS. SHE HAS BROUGHT SO MUCH LOVE TO ALL OUR LIVES I FEEL PROUD TAKING HER OUT IN HER PRAM AND DON'T CARE AT ALL IF PEOPLE STARE,TO ME SHE IS THE BEST THING GOD HAS EVER GIVEN ME AND THE LOVE I FEELFOR HER WILL NEVER BE EQUALLED.IF YOU HAVE A DISABLED CHILD JUST GIVE THEM LOADS OF LOVE AND YOU

Posted on 01/07/2008 at 7:01:48 PM

 
When my daughter was 12 or thirteen, she started developing breakthrough seizures also. It was attributed to puberty due to hormonal changes.

Posted on 01/05/2008 at 9:01:04 PM

 
We have a 5 year old daughter that we still do not and may never have a diagnosis.. she is delayed and had severe low muscle tone at birth.. she just a another MRI that was normal and we are waiting for results of DNA analysis.. we are blessed that she has not had any seizers or other major health issues.. however she cannot talk and still has low muscle tone..While we are very blessed that she is a happy child it is very frustrating when as parents we are not sure of her future. Bless all of you and best of luck with your children

Posted on 11/24/2007 at 8:11:00 AM

 
Hey! I have a 5 year old daughter who was born with microcephely. The docters gave her 2 weeks to live and she is doing great. She also has cp. But what a blessing she is to all of us. Boy is God good!!! I would do it all over again if I could. She is our blessing.

Posted on 09/26/2007 at 5:09:00 PM

 
Rachel, My son was diagnosed at birth w/microcephaly. He has a very rare (only 9 reported cases) chromosome disorder, which is probably why it happened. We were not told to expect much from him by the genetics people. They said he probably won't walk, talk, eat, learn, nothing. 3 years later he is doing ALL of those things. He is delayed in all areas, had 3 years of Early Intervention and now goes to pre-school and additional speech & physical therapy, but he is happy and healthy! It can happen. I don't know what your life or your childs life will be like, but just know that there are positive stories out there. My son is wonderful! We NEVER treated him like he would never do those things. We treated him (as much as we could) like any other child and what he couldn't do we helped with, but we at least made him try. He reached all his milestones late, but he reached them. That's the point!! I recently found childrenwithmicro.org. Maybe they have more info that can help you. You & you

Posted on 08/06/2007 at 2:08:00 PM

 
I'm almost 6 months pregnant and have been told my baby has microcephaly. Everything we have been told indicates that things don't look good for him-and we have been told to consider a termination. The drs are very keen to point out the worst but can not give any definate answers to how severe any problems might be. I don't want our baby to suffer through life but at the same time i could never get rid of a baby in which there is a chance he has a shot at a bareable life. My parents seem to think with all the odds against us that it would be unfair to carry on with the pregnancy. I have no idea where my heads at :-(

Posted on 08/04/2007 at 3:08:00 AM

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