What is Parry-Romberg syndrome?
Parry-Romberg syndrome, also known as Romberg's disease or progressive hemifacial atrophy, is a rare atrophic disorder characterized by a progressive deterioration of the skin and soft tissues of half the face. It typically affects the left side of the face, and is more common in females than in males.
How do you treat Parry-Romberg syndrome?
There is no cure and there are no treatments that can stop the progression of Parry-Romberg syndrome. Reconstructive or microvascular surgery may be needed to repair wasted tissue.
How do you know if you have Parry-Romberg syndrome?
What are the symptoms of Parry-Romberg syndrome?
- the appearance that the mouth and nose are shifting or leaning toward one side.
- a sunken-in appearance of both the eye, as well as the cheek, on the affected side of the face.
Who can diagnose Parry-Romberg syndrome?
How is Parry-Romberg syndrome diagnosed? Doctors at Boston Children's Hospital are able to diagnose this disease based on: a detailed review of your child's complete medical history. an extensive physical examination, looking for signs of progressive loss of skin, fat, muscle, and bone.
Is Parry-Romberg an autoimmune disorder?
An autoimmune mechanism is suspected for Parry-Romberg Syndrome (PRS), however, other research also links infectious diseases to the syndrome. Parry–Romberg syndrome (PRS) is a rare degenerative disease that affects one side of the face called progressive hemifacial atrophy.
Is Parry-Romberg syndrome an autoimmune disease?
Background. Parry–Romberg syndrome (PRS) is a rare disease characterized by progressive unilateral facial atrophy. Its etiology is not well-understood, but the involvement of autoimmunity has been suggested.
Does Parry Romberg affect the brain?
Between 10-20% of individuals with Parry-Romberg syndrome may have changes on brain MRI scans. These changes can include atrophy of the brain on the same side as the facial changes, and sometimes inflammation within the brain itself.