X-Nico

2 unusual facts about CDKL5


Rett syndrome

In less than 10% of RTT cases, mutations in the genes CDKL5 or FOXG1 have also been found to resemble it.

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An atypical form of RTT, characterized by infantile spasms or early onset epilepsy, can also be caused by a mutation to the gene encoding cyclin-dependent kinase-like 5 (CDKL5).


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