8p23.1 duplication syndrome
Meanings
noun
- A rare genetic disorder caused by the duplication of a region from human chromosome 8, leading to one or more of speech delay, developmental delay, congenital heart disease, and mild dysmorphism with prominent forehead and arched eyebrows.
Word forms
Previous
This entry uses open data from Wiktionary (CC BY-SA/GFDL). Word forms are used for search and are not indexed as separate pages.