Witteveen–Kolk syndrome, also known as WITKOS and 15q24 microdeletion syndrome, is a rare neurodevelopmental disorder characterized by developmental delay/intellectual disability, facial dysmorphisms, and short stature.
The syndrome is caused by loss of function of switch‐insensitive 3 transcription regulator family member A (SIN3A).
[1][2] The syndrome was discovered by developmental neuroscientists Josefine S. Witteveen, PhD and Sharon M. Kolk, PhD, in 2016.
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