nestekideskini
Nestekideskini is a rare genetic disorder that affects the development of the brain and nervous system. It is a member of the larger group of disorders known as the 'frontonasal duplication disorders', which are caused by anomalies in the development of the frontonasal prominences during embryonic development.
Symptoms of nestekideskini begin to manifest in infancy and can include altered facial features such as a
The genetic basis of nestekideskini was first described in 2010, and researchers have identified several specific
Diagnosis of nestekideskini typically involves a combination of physical examination, genetic testing, and imaging studies such
Few studies have reported on the incidence and prevalence of nestekideskini, and more research is needed to