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Unilateral polymicrogyria

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Does anyone have a child with unilateral polymicrogyria? My son,

, was originally diagnosed with pacygyria in the left

hemisphere. I sent some MR images to Dr. Dobyns in Chicago and he

thought it was more likely to be polymicrogyria. is not very

handicapped. He met all his milestones and is currently in 1st grade

at a regular school. Recently he has had seizures which have been

described as Lennox-Gastaut. I'm curious to see if there is anyone

out there like my son.

-Steve

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Steve,

Our son has PMG in left hemisphere only and sounds similar to . It

also sounds as though Nathen has done extremely well at school. Do you know

the extent of the PMG on the left side? what's his speech like? Has he got

any weakness down his right side.

is 5 next month and has right sided hemiparisis (weakness) and

struggles terribly with his speech. Other than that he does very well and

understands everything. Epilepsy has been a problem and is quite common in

children with PMG, however he is taking meds and currently has good control.

Hope this helps to know your not alone

Tony and

Unilateral polymicrogyria

> Does anyone have a child with unilateral polymicrogyria? My son,

> , was originally diagnosed with pacygyria in the left

> hemisphere. I sent some MR images to Dr. Dobyns in Chicago and he

> thought it was more likely to be polymicrogyria. is not very

> handicapped. He met all his milestones and is currently in 1st grade

> at a regular school. Recently he has had seizures which have been

> described as Lennox-Gastaut. I'm curious to see if there is anyone

> out there like my son.

> -Steve

>

>

>

>

>

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Hi Steve,

My son is seven and has polymicrogyria on the right side of his brain. He had

done well in school until he began having seizures at age 5 and since then he

has been going downhill and losing skills he previously had. We can't seem to

find a good med to stop the activity. The doctors can't even record much yet -

all they seem to see is subclinical activity. We are trying very hard to find a

solution for him. His motor skills, speech, cognitive ability and emotional

stability have all suffered since the seizures began. Let me know what meds you

have tried.

Joanne

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> Steve,

> Our son has PMG in left hemisphere only and sounds similar to

. It

> also sounds as though Nathen has done extremely well at school. Do

you know

> the extent of the PMG on the left side? what's his speech like? Has

he got

> any weakness down his right side.

> is 5 next month and has right sided hemiparisis (weakness)

and

> struggles terribly with his speech. Other than that he does very

well and

> understands everything. Epilepsy has been a problem and is quite

common in

> children with PMG, however he is taking meds and currently has good

control.

> Hope this helps to know your not alone

> Tony and

>

Thanks for responding. has some trouble with speech. He speaks

slower than most kids his age and he struggles to find words

sometimes. Since the new seizures started, we have noticed a steady

decline in his speech.The seizures were well controlled until lately

when he stated having absence and atonic seizures.

What kind of seizures does your son have? What meds is he on?

-Steve

Unilateral polymicrogyria

>

>

> > Does anyone have a child with unilateral polymicrogyria? My son,

> > , was originally diagnosed with pacygyria in the left

> > hemisphere. I sent some MR images to Dr. Dobyns in Chicago and he

> > thought it was more likely to be polymicrogyria. is not

very

> > handicapped. He met all his milestones and is currently in 1st

grade

> > at a regular school. Recently he has had seizures which have been

> > described as Lennox-Gastaut. I'm curious to see if there is anyone

> > out there like my son.

> > -Steve

> >

> >

> >

> >

> >

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> Hi Steve,

> My son is seven and has polymicrogyria on the right side of his

brain. He had done well in school until he began having seizures at

age 5 and since then he has been going downhill and losing skills he

previously had. We can't seem to find a good med to stop the

activity. The doctors can't even record much yet - all they seem to

see is subclinical activity. We are trying very hard to find a

solution for him. His motor skills, speech, cognitive ability and

emotional stability have all suffered since the seizures began. Let

me know what meds you have tried.

> Joanne

Joanne,

Your son sounds just like . He has recently been having spike

and waves during sleep and some while awake with no clinical

seizures. We didn't know about it until they did an EEG at the right

time. We knew that something was wrong because of the same declines

that you describe, but the doctor we were seeing basically told us we

should be happy that he is function as well as he is. So we dumped

him immediately. Once we found the right doctor he recognized the

problem and stabilized it. After a 2 night stay in the hospital with

IV meds, Ativan, Depakote, and Zonegran and EEG monitoring he was

like a new kid. Everyone who sees him often, like his physical

therapist, could notice a big difference in his motor skills, speech,

emotional and cognitive abilities. Since then, he has done well on

Depakote and Zonegran, although it has only been a couple of weeks.

We are hoping that Zonegran will be the solution. It really important

to have a doctor who has experience with kids like ours. They are

very unique. What meds have you tried? Have you noticed any jerking

or nodding or staring spells? Is he tired often? He could be having

spike and wave during slow sleep which is causing him to not sleep

well and to be sleep deprived which would lower his threshold while

awake and cause similar awake activity. I beleive this is what was

going on with .

-Steve

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