Sabre Sword

Parry-Romberg Syndrome: Autoimmune Horror

Without having surgery , 11-year-old Christine Honeycutt might have been resigned to a lifetime of dramatic deformation and severe neurological trouble. Yet that is precisely what she faces with a rare autoimmune disease called Parry-Romberg syndrome. Her body has started to reject her left side, which caused her face to stop developing when she was five. CNN states that through plastic surgical procedure and immunosuppressant drugs, Honeycutt might be able to live with her Parry-Romberg. Article resource – Surgery saves girl’s face from Parry-Romberg syndrome by MoneyBlogNewz.

Showing a line may be Parry-Romberg syndrome

A line started to go down Christine Honeycutt’s forehead when she was five years old. Her parents thought it was a bruise; her friends thought she had ink on her face. When the mark was nevertheless there after a few weeks, Christine’s mother took her to see a doctor, who prescribed a cream to treat the “discoloration.”. The line didn’t stay faint though. It became clearer over months. In order to get help from a specialist, the Honeycutt’s moved to southern CA from Charlotte, N.C. The Honeycutt’s were given the advice to keep Christine out of the sun though which they had heard before. By the time young Christine Honeycutt was in first grade, abnormal weight gain, fevers and violent seizures began. The left side of her face got really swollen. The right side stayed the very same. Her face has a symmetry start to develop. A few years later, Parry-Romberg syndrome would be what she is clinically determined to have, in 2008.

One out of every million individuals get Parry-Romberg syndrome

One in every 1 million people are diagnose with Parry-Romberg syndrome, or progressive facial hemiatrophy, which females tend to have more often. It is believed that Lincoln may have had it. This is just a guess though. Christine Honeycutt’s immune system was wreaking havoc on her left side, most notably in the face. The “coup de sabre” or “cut of saber” was the line down Christine’s forehead making it look like a sword cut her there. It ended up looking like internet pictures of the disease. There were found when searching Parry-Romberg syndrome.

“There were horrifying pictures,” said Vicki Honeycutt, Christine’s mother. “One side [of a patient's face] was a skeleton and the other side wasn’t.”

No treatment, conserve reconstructive surgical procedure and continuing treatments

Curing Parry-Romberg syndrome isn’t possible. There is no treatment currently. Facial reconstructive surgery and immunosuppressant drugs can be beneficial, as has been the case so far for Christine Honeycutt. It took about seven hrs for the Extensive plastic surgery to be done. She is getting closer to regular. There is nevertheless some swelling, however not enough to keep Christine away from school.

“I like my nose better now,” she said.

Information from

CNN

cnn.com/2011/HEALTH/02/25/surgery.parry.romberg.disorder/

National Institute of Neurological Disorders and Stroke

ninds.nih.gov/disorders/parry_romberg/parry_romberg.htm

PRS Resource

prsresource.com/

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