ZTTK syndrome is an ultrarare neurodevelopmental disorder, that was only discovered in 2016. There are only 50+ patients identified in the scientific literature today and no known treatments/cures All documented cases of ZTTK syndrome are de novo mutation resulting in haploinsufficiency, with a complex and highly varied multi-system phenotype. The most prevalent symptoms include global developmental delay (gross motor, feeding, and speech delays), intellectual disability, and seizures (~50% of the known population)
| Website | https://www.zttk.org |
| Employees | 2 (0 on RocketReach) |
| Founded | 2023 |
| Industry | Biotechnology Research |
| Keywords | Rare Disease Research, Orphan Diseases, Genetic Disorder Research, Pediatric Neurology, Rare Disease Advocacy, Genetic Mutations, Molecular Genetics, Clinical Research, Patient Advocacy, Genome Sequencing, Medical Research, Gene Therapy, Precision Medicine, Personalized Medicine, New Treatments |
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