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040-68334455Frequently Asked Questions
What is Miller Syndrome?
Miller Syndrome, also known as postaxial acrofacial dysostosis, is a rare genetic disorder that affects facial and limb development.
What are the common symptoms of Miller Syndrome?
Common symptoms of Miller Syndrome include underdeveloped or absent cheekbones, small jaw, cleft palate, and abnormalities in the hands and feet.
How is Miller Syndrome diagnosed?
Miller Syndrome is usually diagnosed through physical examination, medical history review, imaging tests like X-rays, and molecular genetic testing.
Is there a cure for Miller Syndrome?
There is no cure for Miller Syndrome. Treatment focuses on managing symptoms and may involve surgeries to correct facial and limb abnormalities.
What is the prognosis for individuals with Miller Syndrome?
Prognosis for individuals with Miller Syndrome varies depending on the severity of symptoms. Early intervention and ongoing medical care can help improve quality of life.
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