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040-68334455Frequently Asked Questions
What is Sanderson–Fraser Syndrome?
Sanderson–Fraser Syndrome, also known as cerebrooculofacioskeletal syndrome, is a rare genetic disorder that affects various parts of the body including the brain, eyes, and bones.
What are the common symptoms of Sanderson–Fraser Syndrome?
Common symptoms include intellectual disability, growth retardation, facial abnormalities, vision problems, and skeletal abnormalities.
Is there a specific treatment for Sanderson–Fraser Syndrome?
Currently, there is no specific treatment for Sanderson–Fraser Syndrome. Management focuses on addressing individual symptoms and providing supportive care.
What is the prognosis for individuals with Sanderson–Fraser Syndrome?
The prognosis for individuals with Sanderson–Fraser Syndrome varies depending on the severity of symptoms. Regular medical monitoring and intervention can help improve quality of life.
Is Sanderson–Fraser Syndrome inherited?
Sanderson–Fraser Syndrome is inherited in an autosomal recessive pattern, meaning that both parents must carry a copy of the mutated gene for a child to develop the condition.
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