https://rarediseases.info.nih.gov/diseases/10216/microhydranencephaly
It’s basically a genetic disease by whom the affected individual has a slower brain development. Apparently, this is caused by a mutation in the NDE1 gene, which codes proteins that are located in the centrosomes, which manage microtubules and cell overall structure. One could only imagine the possible consequences of mutations in such a gene.
https://ghr.nlm.nih.gov/gene/NDE1
Funny comment on the gene name
Huh, NudE, haha, funy.
Any thoughts or any other genes/genetic diseases you want to share?