Joubert Foundation's logo |
Describing Joubert syndrome, medically, can be daunting, so for this post I'll quote the Joubert Syndrome & Related Disorders Foundation's website, adding in the occasional photo or point for context:
Joubert syndrome is a rare genetic disorder characterized by decreased muscle tone, difficulties with coordination, abnormal eye movements, abnormal breathing patterns and intellectual disability. These issues are due to abnormal brain development, resulting in decreased size of the cerebellar vermis and other brain abnormalities that appear as the “molar tooth sign” on a brain MRI.
Molar tooth in MRI |
Although rare, several hundred individuals with Joubert syndrome have been reported in the medical literature. Mutations in at least 22 genes cause Joubert syndrome, accounting for ~60% of patients. (My causative gene is still unknown.) Subsets of individuals with Joubert syndrome can also have polydactyly (extra fingers or toes) , as well as retinal, kidney and liver disease requiring medical intervention.
Former sixth finger, now "bump" on my left hand |
During this summer's JS conference in Phoenix, I attended a "science fair" with researchers studying cilia. Very interesting stuff, and the researchers were eager to meet individuals impacted by their studies.
Currently, Joubert syndrome affects an estimated 1 in 80 000 individuals worldwide and about 1000 families are known to the Foundation.
If you're interested in learning more, visit the Joubert Syndrome & Related Disorders Foundation's website at https://jsrdf.org/
Cheers!
Thanks Scott!
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