ZTTK SON-Shine Foundation

Zttk son-shine foundation email format

Verified email-pattern data for Zttk Son-Shine Foundation is currently limited. You can still use the company insights and contact sections below.
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)
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