8p23.1 duplication syndrome
8p23.1 duplication syndrome 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.
Noun
8p23.1 duplication syndrome (uncountable)
- 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.
Questions about 8p23.1 duplication syndrome
- What does 8p23.1 duplication syndrome mean?
- 8p23.1 duplication syndrome means 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.
- What part of speech is 8p23.1 duplication syndrome?
- 8p23.1 duplication syndrome is a noun.
Words near 8p23.1 duplication syndrome in the dictionary
Source and license
Adapted from Wiktionary: 8p23.1 duplication syndrome (page history and authors). Text available under the Creative Commons Attribution-ShareAlike 4.0 license. Word.ws reformatted the entry and added links. Wiktionary data of 2026-09-02.
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Cite this entry: “8p23.1 duplication syndrome.” Word.ws, https://word.ws/8p23.1_duplication_syndrome. Based on Wiktionary, CC BY-SA 4.0.
