rare disorder makes girl's skull too small for brain

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Rare disorder makes girl's skull too small for brain Allie Barone, 6, smiles for the camera while receiving IV antibiotics at her Clinton, N.Y. home. (Courtesy of Stephanie Barone) Allie's beaded stitches, which she hopes to have removed at the end of the month. (Courtesy

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Allie Barone, 6, smiles for the camera while receiving IV antibiotics at her Clinton, N.Y. home. (Co...

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Page 1: Rare disorder makes girl's skull too small for brain

Rare disorder makes girl's skull too small for brain

Allie Barone, 6, smiles for the camera while receiving IV antibiotics at her Clinton, N.Y. home.(Courtesy of Stephanie Barone)

Allie's beaded stitches, which she hopes to have removed at the end of the month. (Courtesy

Page 2: Rare disorder makes girl's skull too small for brain

Stephanie Barone)

Allie colors at the hospital with her sister Claire. (Courtesy Stephanie Barone)

Despite being in the hospital for nearly three weeks, Allie kept a happy smile on her face. (CourtesyStephanie Barone)

Page 3: Rare disorder makes girl's skull too small for brain

A picture of Allie's artwork, which she drew during her hospital stay. (Courtesy Stephanie Barone)

Six-year-old Allie Barone had been suffering from severe headaches for a few years -- and since herfamily has a history of epilepsy and migraines, her mother, Stephanie, decided it was finally time tosee a specialist.

An MRI revealed Allie had Type I Chiari malformation, which meant the back of her skull was toosmall for its contents.

"Essentially, what happens, the cerebellum tonsils are pushing through the bottom of the skull andpotentially putting pressure on the spinal cord and the tissue of the spinal cord," said Dr. RobertKeating, professor and chief of neurosurgery at Children's National Medical Center in Washington,D.C.

Allie, who lives in Clinton, N.Y., initially went to the Chiari Institute on Long Island, but her parentsdecided to see Keating for a second opinion.

Keating said the symptoms, which are multiple and vary depending on the patients' age, includeheadaches and occipital headaches (often made worse by excursion such as running or evensneezing), neurological issues or double vision, and/or the feeling of pins and needles in the legs.

Approximately one percent of the U.S. population has Chiari malformation -- and Keating said it's notjust kids who are being diagnosed these days; adults in their 20s and 30s are being diagnosedincidentally.

Chiari malformations can be caused by structural defects in the brain and spinal cord, according tothe National Institute of Neurological Disorders and Stroke, or can be caused if too much spinal fluidis drained from the back in cases of injury. Patients like Allie may just have a genetic predisposition.

Not all Type I Chiari malformations present with symptoms, and there are at least three other types

Page 4: Rare disorder makes girl's skull too small for brain

of malformations (Type II usually involves a form of spina bifida; Type III is the most serious andcauses severe neurological defects; Type IV may have parts of the cerebellum missing and parts ofthe skull and spinal cord may be visible to the naked eye).

"Her brain stem was compressed and squished through the opening of the base of her skull, wherethe skull meets the spinal cord; it's supposed to be wide open," Stephanie Barone said. "When thespinal fluid couldn't get into her brain, that's why she had the headaches."

Barone said she and her husband, Rob (who also have another daughter, Claire, 8), decided to gowith Keating for what they thought would be a simple surgery. They checked into the hospital onAug. 1.

During the decompression procedure, Keating went in through the neck and removed some of thebone.

Using ultrasound, he opened the covering to her brain. Under the microscope, he saw there wereobstructions to the spinal fluid, so he cut those out too. The whole process took about three or fourhours.

However, in a rare event, Allie began leaking spinal fluid from her incision about three or four daysafter that initial surgery, so Keating took her back into surgery.

"Now that we had opened the covering and put a patch on, it was leaking through the patch," hesaid. "Our goal was to go in and reinforce the stitches, and at the same time, place a tube in herlower back so we could divert the spinal fluid and let the neck heal."

Meanwhile, Allie was starting to feel better. She was sitting up and drawing, which is her favoritepastime, and the family still hoped for a speedy discharge.

Page 5: Rare disorder makes girl's skull too small for brain

However, just when it looked like shewas healing, and Keating started toreduce the drainage from the tube, shebegan leaking spinal fluid again. A thirdsurgery would have to be performed.

"The feeling is, 'Why are we havingissues?'" Keating said. "The answer was,she had hydrocephalus, or too muchwater in the brain. We needed to put ashunt in to remove the excess water."

This went well for the next few days,and the Barones were literally goingover discharge papers as Allie sat atable drawing, bent over. But every timeAllie looked up, they noticed the leakageonce again.

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Artwork provides insight

"She'd look down at her drawing, and then look up; and it would drip down the back of her neck,"Barone said. "She just said, 'It's dripping again, Mommy;' and we both knew it meant we weren'tleaving the next morning, and that she needed another surgery. ...It was a heartbreaking hour forboth of us, and then turned out to be what finally helped the doctors find the problem and get ushome."

Keating's colleague performed the fourth surgery, who told Barone that while the standard way ofperforming the surgery was to lie the patient face down, she had decided to sit Allie up -- like shewas drawing -- and that's when doctors noticed her second vertebrae was also abnormally shapedand acting like a knife, scraping the dura (the outer layer of three membranes that surround thebrain and spinal cord).

"It was another abnormality that no one knew about," said Barone, who credits Keating and his teamfor making her daughter as if nothing ever happened. "She started school (last week) and she hasmore energy than ever. She's like a whole new kid."

Allie will have to return to D.C. for a checkup at the end of September. Her beaded stitches will beremoved then, and hopefully some of her restrictions will be lifted at that point.

"My thing is, I learned from this," Barone said. "Do your homework, advocate and be your owndoctor, too. Get a second opinion; talk to which doctor and find which procedure you arecomfortable with for your kid."

Keating said patients with Chiari malformations can go back to their usual activities rather quickly --in Allie's case, she's looking forward to skiing with her sister.

Page 6: Rare disorder makes girl's skull too small for brain

While there is data to back up a 10-year success rate, there aren't numbers for longer than that,Keating said.Â

"But that doesn't mean I'm not optimistic," he added.

Keating is pleased with Allie's overall outcome, and he stressed that most Chiari cases do not involveso many surgeries.

"She's quite a character," he said. "I'm looking forward to her long-term prognosis."

Click here to check out Allie's artwork on Facebook.

http://www.foxnews.com/health/2012/09/11/rare-disorder-makes-girl-skull-too-small-for-brain/