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Christianson Syndrome - FAQs

Q: How does Christianson syndrome occur?

A: Christianson syndrome occurs due to changes in a particular gene called SLC9A6. The condition runs in families and is inherited through the X chromosome.

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Q: How is Christianson syndrome passed to the offspring?

A: Christianson syndrome is inherited through the X chromosome. In males each cell contains one X and one Y chromosomes, while females have two X chromosomes. So, in males if the X chromosome is affected, the individual exhibits signs of Christian Syndrome. But in females, both the X chromosomes have to be affected to exhibit the symptoms of Christianson Syndrome.

Q: How common is Christianson syndrome?

A: Christianson syndrome is an extremely rare condition.

Q: How is Christianson syndrome treated?

A: Treatment involves maintenance with symptomatic care, as no specific treatment is available for this condition.


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