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Joubert Syndrome is a combination of brain abnormalities, that together are known as the molar tooth sign. Symptoms of this genetic disorder may vary from person to person

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The condition could be caused by mutations in more than 30 genes. Mutations in the genes associated with Joubert syndrome lead to problems with the structure and function of the cells. Yes, it can be inherited.

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There are many symptoms that follow along with having Joubert Syndrome. Some include:
-extra toes and fingers
-kidney disease
-vision loss
-triangle shaped mouth
-hormone problems
-wide/broad forehead

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Joubert syndrome effects 1 in 80,000 and 1 in 100,000 newborns. It has become more common in certain ethnic groups such as Ashkenazi Jewish, French-Canadian, and Hutterite. More research needs to be done since it has such a wide range of symptoms, so it is still in the category of under diagnosed.

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There are a lot of things that affect treatment for a human carrier of Joubert Syndrome. Every patient is different of unique in some way which already makes it tougher to tackle. So far, treatment medicine is still in the developing phase.

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A cure for the disorder is being developed, but since it is not a very well known genetic disorder, progress is slower to develop a cure/treatment medicine since there are not as many scientists or doctors helping out to make a good cure compared to other notorious diseases.

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- Joubert Syndrome is also known as CORS, JBTS, and other nicknames.
- In some remaining cases of Joubert Syndrome, some genetic causes are still unknown
- It can also be linked to a molar tooth sign because of its brain abnormalities, that under an MRI result in a cross section of a molar tooth.

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Joubert Syndrome can make an individual's life harder by making your vision worse, or it could give you with a lower muscle tone if you were born with the syndrome and have carried it your whole life.